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Last Updated: November 5, 2024

CLINICAL TRIALS PROFILE FOR MANNITOL 25%


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All Clinical Trials for MANNITOL 25%

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00003062 ↗ Temozolomide in Patients With Progressive or Recurrent Non-small Cell Lung Cancer Completed European Organisation for Research and Treatment of Cancer - EORTC Phase 2 1997-07-01 RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effect of temozolomide in patients with progressive or recurrent stage IV non-small cell lung cancer, with or without brain metastases, who have not been treated for metastatic disease with chemotherapy.
NCT00004767 ↗ Phase II Study of Sodium Phenylbutyrate, Sodium Benzoate, Sodium Phenylacetate, and Dietary Intervention for Urea Cycle Disorders Completed Johns Hopkins University Phase 2 1985-01-01 OBJECTIVES: I. Assess the safety and efficacy of sodium phenylbutyrate, sodium benzoate, sodium phenylacetate, and dietary intervention in patients with urea cycle disorders.
NCT00004767 ↗ Phase II Study of Sodium Phenylbutyrate, Sodium Benzoate, Sodium Phenylacetate, and Dietary Intervention for Urea Cycle Disorders Completed National Center for Research Resources (NCRR) Phase 2 1985-01-01 OBJECTIVES: I. Assess the safety and efficacy of sodium phenylbutyrate, sodium benzoate, sodium phenylacetate, and dietary intervention in patients with urea cycle disorders.
NCT00111956 ↗ Effects of Tumor Necrosis Factor (TNF)-Alpha Antagonism in Patients With Metabolic Syndrome Completed Massachusetts General Hospital Phase 2/Phase 3 2004-04-01 Metabolic syndrome is associated with increased inflammatory cytokines and reduced adiponectin, that may be mediated in part by TNF production from abdominal fat. We reasoned that an anti-TNF agent would reduce C-reactive protein (CRP) and increase adiponectin, improving the inflammatory milieu associated with metabolic syndrome.
NCT00111956 ↗ Effects of Tumor Necrosis Factor (TNF)-Alpha Antagonism in Patients With Metabolic Syndrome Completed National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Phase 2/Phase 3 2004-04-01 Metabolic syndrome is associated with increased inflammatory cytokines and reduced adiponectin, that may be mediated in part by TNF production from abdominal fat. We reasoned that an anti-TNF agent would reduce C-reactive protein (CRP) and increase adiponectin, improving the inflammatory milieu associated with metabolic syndrome.
NCT00113854 ↗ Mannitol as Adjunct Therapy for Childhood Cerebral Malaria Unknown status Makerere University Phase 3 2004-10-01 Cerebral malaria is a life-threatening complication of Plasmodium falciparum infection in African children and nonimmune travellers despite availability of quinine, the current drug of choice. Several reports have suggested that raised intracranial pressure (ICP) is a major cause of death among children with cerebral malaria. Mannitol, an osmotic diuretic, effectively lowers ICP and is used to treat post traumatic raised ICP. There have been some case reports of reduction in mortality and morbidity in African children with cerebral malaria following administration of mannitol, but as these were not randomized controlled trials it is difficult to evaluate their significance. This study seeks to establish whether a single dose of intravenous mannitol given to children with cerebral malaria will significantly reduce the coma recovery time.
NCT00117182 ↗ Aridol Challenge as a Tool to Predict Treatment Response to Inhaled Corticosteroids in COPD Completed Pharmaxis Phase 2 2005-07-01 The purpose of this study is to determine whether the Aridol (mannitol) challenge test can predict response to treatment with inhaled corticosteroids in COPD subjects. Subjects will undergo an Aridol test and then 3 months of treatment with inhaled corticosteroids. The effect on lung function and quality of life will then be measured and correlated with the Aridol test result.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for MANNITOL 25%

Condition Name

Condition Name for MANNITOL 25%
Intervention Trials
Asthma 20
Cystic Fibrosis 10
Healthy 7
Glioblastoma Multiforme 6
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Condition MeSH

Condition MeSH for MANNITOL 25%
Intervention Trials
Asthma 23
Intracranial Hypertension 12
Brain Neoplasms 10
Fibrosis 10
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Clinical Trial Locations for MANNITOL 25%

Trials by Country

Trials by Country for MANNITOL 25%
Location Trials
United States 137
Canada 38
United Kingdom 35
Australia 34
Italy 20
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Trials by US State

Trials by US State for MANNITOL 25%
Location Trials
New York 19
Massachusetts 12
Minnesota 9
Oregon 8
Ohio 7
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Clinical Trial Progress for MANNITOL 25%

Clinical Trial Phase

Clinical Trial Phase for MANNITOL 25%
Clinical Trial Phase Trials
Phase 4 37
Phase 3 34
Phase 2/Phase 3 10
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Clinical Trial Status

Clinical Trial Status for MANNITOL 25%
Clinical Trial Phase Trials
Completed 132
Unknown status 27
Not yet recruiting 18
[disabled in preview] 44
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Clinical Trial Sponsors for MANNITOL 25%

Sponsor Name

Sponsor Name for MANNITOL 25%
Sponsor Trials
Pharmaxis 19
Northwell Health 7
National Cancer Institute (NCI) 6
[disabled in preview] 21
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Sponsor Type

Sponsor Type for MANNITOL 25%
Sponsor Trials
Other 366
Industry 64
NIH 17
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