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Last Updated: March 30, 2025

CLINICAL TRIALS PROFILE FOR SODIUM NITROPRUSSIDE


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All Clinical Trials for SODIUM NITROPRUSSIDE

Trial IDTitleStatusSponsorPhaseStart DateSummary
NCT00072826 ↗ Atorvastatin Therapy to Improve Endothelial Function in Sickle Cell Disease Completed National Institutes of Health Clinical Center (CC) Phase 1 2003-11-04 This study will examine the effects of oral atorvastatin on the linings of blood vessels in patients with sickle cell disease, plus the agent's effect on blood markers of inflammation and blood vessel function. Sickle cell disease is a recessive genetic disorder and the most common genetic disease affecting African Americans. Inherited are abnormal genes that make hemoglobin, the substance within red blood cells that carries oxygen from the lungs to the body. In the disease, sickle hemoglobin leads to rigidity or hardness of the red cells, causing obstruction in small blood vessels, inflammation, and injury to organs when the flow of blood to them is blocked. Some medications already prescribed for other diseases, such as atorvastatin, which is used for lowering cholesterol levels, can improve blood flow. Patients 18 to 65 years of age who have sickle cell disease, who have not had an acute pain episode within the previous week, and who are not pregnant or lactating may be eligible for this study. They will undergo a complete medical history; physical examination; baseline blood tests; and echocardiogram, in which an ultrasound wand is placed against the chest wall to get images inside the heart and blood vessels. In addition, patients will have blood flow studies. During the procedure, they will lie in an adjustable reclining chair for 5 to 6 hours. There will be 20- to 30-minute rests between specific activities and blood samples will be drawn intermittently for testing. Small tubes will be placed in the artery of the forearm at the inside of the elbow. Normal saline will be infused into one tube. A small pressure cuff will be applied to the wrist and a larger cuff to the upper arm. Both cuffs will be attached to an inflation device. A device like a rubber band, a strain gauge, will be placed around the widest part of the forearm. When the pressure cuffs are inflated, blood will flow into the arm, stretching the gauge proportion to blood flow, and information will be recorded. Then light reflected from the patients' hand and the blood flow in the forearm will be measured. Activity of the genes in the white blood cells will be measured as well. Small amounts of sodium nitroprusside, widely used to reduce blood pressure in people with dangerously high blood pressure, will be injected and blood flow will be measured. Later, small amounts of acetylcholine will be injected. It usually causes blood vessels to expand. After that, small amounts of L-NMMA will be injected. It usually decreases local blood flow by blocking the production of nitric oxide in the cells lining the arm's blood vessels. Then acetylcholine combined with L-NMMA will be injected. After that, oxypurinol, an agent taken by many patients to prevent gout, will be injected. The procedures will be repeated, with oxypurinol given along with each of the agents, and the measurement of blood flow in the forearm will be measured after each drug combination. Afterward, patients will be treated for 4 weeks at home with oral atorvastatin. They will be asked to visit the Clinical Center every 2 weeks for collection of blood samples and an examination. After 4 weeks of taking atorvastatin orally, they will be asked to return to repeat the blood flow studies, but only the first half will be conducted. The part using oxypurinol will not be needed. Regarding some of the blood samples collected during the study, there will be an examination of the genes found in the white blood cells. Specific attention will go to those genes that make proteins for cell-to-cell interaction and inflammation, plus those that cause blood cells to stick to the lining of blood vessels.
NCT00009581 ↗ Nitric Oxide to Improve Blood Flow in Sickle Cell Disease Completed National Institutes of Health Clinical Center (CC) Phase 2 2001-01-01 Nitric oxide is important in regulating blood vessel dilation, and consequently, blood flow. This gas is continuously produced by cells that line the blood vessels. It is also transported from the lungs by hemoglobin in red blood cells. This study will examine how this gas regulates blood vessels and blood flow in people with sickle cell anemia. It will also look at a possible benefit of using certain genetic information to compare the white blood cells of people with sickle cell anemia to those without the disease. Patients with sickle cell anemia and healthy normal volunteers 18 to 65 years of age may be eligible for this study. Candidates will be screened with a medical history, cardiovascular physical examination, electrocardiogram and routine blood tests. Participation of volunteers without sickle cell anemia will be limited to a single blood draw for genetic study. Sickle cell disease patients will undergo the following procedures: Patients will lie in a reclining chair during the study. After administration of a local anesthetic, small tubes will be inserted through a needle into the artery and vein of the patient's forearm. These are used to measure blood pressure and draw blood samples during the study. Forearm blood flow will be measured using pressure cuffs placed on the wrist and upper arm, and a strain gauge (a rubber band device) placed around the forearm. When the cuffs are inflated, blood flows into the arm, stretching the strain gauge, and the flow measurement is recorded. A small lamp will be positioned over the hand. Light reflected back from the hand provides information about nitric oxide and hemoglobin in the blood of the skin. A squeezing device called a dynamometer will be used to measure handgrip strength. Baseline blood flow, nitric oxide, hemoglobin, and handgrip will be measured after an infusion of glucose (sugar) and water. These measurements will be repeated at various times before, during and after administration of small doses of the following drugs: - Sodium nitroprusside - causes blood vessels to dilate and increases blood flow to the heart - Acetylcholine - causes blood vessels to dilate and slows heart rate - LNMMA - decreases blood flow by blocking the production of nitric oxide There will be a 20- to 30-minute rest period between injections of the different drugs. When the above tests are completed, the patient will breathe a mixture of room air and nitric oxide for 1 hour through a facemask placed over the face, after which forearm blood flow and light reflected from the hand will be measured. Then the patient will do the handgrip exercise for 5 minutes, after which blood flow and hand lamp measurements will be taken. After a 20-minute rest period (with continued breathing of room air/nitric oxide), L-NMMA will be infused again. The handgrip exercise, blood flow and hand lamp measurements will be repeated. The face mask will then be removed, and the tubes will be removed 20 minutes later. Blood samples will be collected at various times during the 5- to 6-hour study through the tubes in the arm. Some of the blood will be used to look at genes that make proteins involved in cell-to-cell communication, inflammation, and in making red and white blood cells stick to the lining of blood vessels.
NCT00004575 ↗ Effects of Miconazole on Blood Flow Completed National Heart, Lung, and Blood Institute (NHLBI) Phase 1 2000-02-01 This study will investigate the effect of the drug miconazole on blood vessel dilation. Miconazole stops production of EDHF, a substance that causes arteries to dilate. EDHF is produced by the cells that line blood vessels. Normal volunteers between the ages of 21 to 60 may participate in this study. Candidates will be screened for eligibility with a medical history, physical examination, electrocardiogram and routine laboratory tests. Those enrolled will be injected with miconazole to study its effects on blood vessels. Study participants will take three aspirin tablets. After administration of a local anesthetic, small tubes will be inserted through a needle into the artery and vein of the forearm. These will be used to measure blood pressure and to draw blood samples during the study. Forearm blood flow will be measured using pressure cuffs placed on the wrist and upper arm, and a strain gauge (a rubber band device) placed around the forearm. When the cuffs are inflated, blood will flow into the arm, stretching the strain gauge, and the flow measurement will be recorded. Small doses of four drugs-bradykinin, sodium nitroprusside, miconazole, and LNMMA-will be given through the arterial catheter. Bradykinin stimulates the release of EDHF and can lower blood pressure. Sodium nitroprusside causes blood vessels to dilate and is used to treat high blood pressure and heart failure. Miconazole is commonly prescribed to treat various infections, including vaginal yeast infections, jock itch and athlete's foot. In much higher doses, it is used to treat fungal infections that have spread to the lungs, brain, kidneys, or bladder. LNMMA inhibits production of nitric oxide, another substance produced by the lining cells of blood vessels. Blood flow will be measured throughout the study, which will last approximately 3 hours.
>Trial ID>Title>Status>Phase>Start Date>Summary
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Clinical Trial Conditions for SODIUM NITROPRUSSIDE

Condition Name

765001234567HealthyVasodilationHypertension[disabled in preview]
Condition Name for SODIUM NITROPRUSSIDE
Intervention Trials
Healthy 7
Vasodilation 6
Hypertension 5
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Condition MeSH

65400123456HypertensionAnemia, Sickle CellST Elevation Myocardial Infarction[disabled in preview]
Condition MeSH for SODIUM NITROPRUSSIDE
Intervention Trials
Hypertension 6
Anemia, Sickle Cell 5
ST Elevation Myocardial Infarction 4
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Clinical Trial Locations for SODIUM NITROPRUSSIDE

Trials by Country

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Trials by Country for SODIUM NITROPRUSSIDE
Location Trials
United States 68
United Kingdom 9
Brazil 8
Canada 5
China 4
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Trials by US State

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Trials by US State for SODIUM NITROPRUSSIDE
Location Trials
Maryland 8
Texas 5
New York 5
Tennessee 4
California 4
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Clinical Trial Progress for SODIUM NITROPRUSSIDE

Clinical Trial Phase

35.7%10.7%53.6%00246810121416Phase 4Phase 3Phase 2[disabled in preview]
Clinical Trial Phase for SODIUM NITROPRUSSIDE
Clinical Trial Phase Trials
Phase 4 10
Phase 3 3
Phase 2 15
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Clinical Trial Status

66.1%17.9%16.1%00510152025303540CompletedTerminatedRecruiting[disabled in preview]
Clinical Trial Status for SODIUM NITROPRUSSIDE
Clinical Trial Phase Trials
Completed 37
Terminated 10
Recruiting 9
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Clinical Trial Sponsors for SODIUM NITROPRUSSIDE

Sponsor Name

trials01234567National Heart, Lung, and Blood Institute (NHLBI)Vanderbilt University Medical CenterColorado State University[disabled in preview]
Sponsor Name for SODIUM NITROPRUSSIDE
Sponsor Trials
National Heart, Lung, and Blood Institute (NHLBI) 7
Vanderbilt University Medical Center 3
Colorado State University 3
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Sponsor Type

73.9%13.9%12.2%00102030405060708090OtherNIHIndustry[disabled in preview]
Sponsor Type for SODIUM NITROPRUSSIDE
Sponsor Trials
Other 85
NIH 16
Industry 14
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Sodium Nitroprusside: Clinical Trials, Market Analysis, and Projections

Clinical Trials and Efficacy

Overview of Sodium Nitroprusside

Sodium nitroprusside (SNP) is a potent vasodilator that has been used for several decades to manage acute hypertensive crises, acute heart failure, and to induce controlled hypotension during surgery. Recently, it has also been investigated for its potential in treating schizophrenia due to its role as a nitric oxide donor.

Clinical Trials for Schizophrenia

Studies on the efficacy of sodium nitroprusside in treating schizophrenia have yielded mixed results. A meta-analysis of six randomized controlled trials involving 174 patients found no statistically significant benefit of sodium nitroprusside over placebo in terms of the Positive and Negative Syndrome Scale (PANSS) total and Brief Psychiatric Rating Scale (BPRS-18) scores. However, there was a slight significant difference in PANSS positive scores, suggesting some efficacy in alleviating positive symptoms of schizophrenia, although this finding was not consistent across all studies[1].

Safety and Adverse Effects

The safety profile of sodium nitroprusside is a significant concern. Clinical trials and post-marketing reports have highlighted several adverse effects, including excessive hypotension, carboxyhemoglobinemia, and visual impairment. In pediatric patients, the FDA has identified a safety signal for carboxyhemoglobinemia, which can be life-threatening[3].

Market Analysis

Market Size and Growth

The Sodium Nitroprusside API Market has experienced substantial growth in recent years. As of 2023, the market size was valued at approximately USD 0.16 billion and is projected to reach USD 0.24 billion by 2030, with a Compound Annual Growth Rate (CAGR) of 5.2%[5].

Market Segmentation

The market is segmented based on type (0.98, 0.99, and others), application (Medical Pharmaceutical and Scientific Research), and geography (North America, Europe, Asia-Pacific, South America, and Middle-East and Africa). The increasing demand for sodium nitroprusside API in medical and research applications is driving the market growth[2][5].

Key Players

The market is dominated by several key players, including Hainan Poly Pharm, ChemWerth Inc, Biophore India Pharmaceuticals, Tecoland Corporation, Amphastar Pharmaceuticals, and others. These companies are evaluated based on their product offerings, financial statements, strategic approaches, and geographical penetration[5].

Market Projections

Forecast Period

From 2023 to 2030, the Sodium Nitroprusside API Market is expected to exhibit robust growth driven by increasing demand in medical and research sectors. The market dynamics are influenced by factors such as product pricing, market penetration, country GDP, and regulatory environments[5].

Drivers and Challenges

The growth of the market is driven by the need for effective antihypertensive and vasodilatory agents in clinical settings. However, challenges such as adverse effects, toxicity, and the emergence of newer agents may impact the market. A thorough analysis of Porter's 5 Forces Framework, macroeconomic evaluation, and value chain scrutiny highlights the complexities of the market[2][5].

Geographical Analysis

The market is geographically segmented, with North America, Europe, and Asia-Pacific being key regions. The growth in these regions is attributed to advanced healthcare infrastructure, increased research activities, and higher demand for pharmaceutical products[5].

Clinical and Market Implications

Clinical Use

Sodium nitroprusside remains a critical drug in managing acute hypertensive crises, acute heart failure, and inducing controlled hypotension during surgery. Its use in pediatric patients is also established, although it requires careful monitoring due to potential adverse effects[3][4].

Market Opportunities

The growing demand for sodium nitroprusside API presents opportunities for pharmaceutical companies to expand their product portfolios and invest in research and development. However, companies must also address the safety concerns and develop strategies to mitigate adverse effects[5].

"Sodium nitroprusside is an antihypertensive drug that releases blood vessels by releasing carbon monoxide, which might have the ability to regulate N-methyl-D-aspartate and intermediate metabolites"[1].

Key Takeaways

  • Clinical Trials: Sodium nitroprusside shows limited efficacy in treating schizophrenia but significant benefits in managing hypertensive crises and acute heart failure.
  • Market Growth: The Sodium Nitroprusside API Market is projected to grow at a CAGR of 5.2% from 2023 to 2030.
  • Safety Concerns: The drug is associated with several adverse effects, including excessive hypotension and carboxyhemoglobinemia.
  • Market Segmentation: The market is segmented by type, application, and geography, with key players dominating the landscape.
  • Geographical Analysis: North America, Europe, and Asia-Pacific are key regions driving market growth.

FAQs

What are the primary clinical uses of sodium nitroprusside?

Sodium nitroprusside is primarily used to manage acute hypertensive crises, treat acute heart failure, and induce controlled hypotension during surgery[3][4].

What are the potential adverse effects of sodium nitroprusside?

The drug can cause excessive hypotension, carboxyhemoglobinemia, and visual impairment. In pediatric patients, it has been associated with serious adverse events[3].

What is the projected market size of the Sodium Nitroprusside API Market by 2030?

The market is expected to reach USD 0.24 billion by 2030, growing at a CAGR of 5.2% from 2023[5].

Which regions are driving the growth of the Sodium Nitroprusside API Market?

North America, Europe, and Asia-Pacific are the key regions driving the market growth due to advanced healthcare infrastructure and increased research activities[5].

Who are the key players in the Sodium Nitroprusside API Market?

Key players include Hainan Poly Pharm, ChemWerth Inc, Biophore India Pharmaceuticals, and others, which are evaluated based on their product offerings and strategic approaches[5].

Sources

  1. Frontiers in Psychiatry: "The efficacy and safety of sodium nitroprusside in the treatment of schizophrenia: A systematic review and meta-analysis."
  2. Market Research Intellect: "Sodium Nitroprusside API Market Size, Scope And Forecast Report."
  3. FDA: "Nitropress® (sodium nitroprusside) injection."
  4. The Cardiology Advisor: "Nitroprusside."
  5. Verified Market Reports: "Sodium Nitroprusside API Market Size, Share, Trends."

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