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Last Updated: November 22, 2024

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CLINICAL TRIALS PROFILE FOR SODIUM POLYSTYRENE SULFONATE


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All Clinical Trials for SODIUM POLYSTYRENE SULFONATE

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00004328 ↗ Phase II Study of the Pathophysiology and Treatment With Enalapril and Polystyrene Sulfonate for Pseudohypoaldosteronism, Type I Completed University of Texas Phase 2 1992-12-01 OBJECTIVES: I. Establish the sodium and potassium intake that will maintain a normovolemic state in a patient with pseudohypoaldosteronism. II. Determine the effect of extracellular fluid volume and serum potassium manipulations on exercise tolerance, cardiac function, and endurance. III. Investigate pharmacologic methods of limiting excretion of sodium in urine and sweat.
NCT00004328 ↗ Phase II Study of the Pathophysiology and Treatment With Enalapril and Polystyrene Sulfonate for Pseudohypoaldosteronism, Type I Completed National Center for Research Resources (NCRR) Phase 2 1992-12-01 OBJECTIVES: I. Establish the sodium and potassium intake that will maintain a normovolemic state in a patient with pseudohypoaldosteronism. II. Determine the effect of extracellular fluid volume and serum potassium manipulations on exercise tolerance, cardiac function, and endurance. III. Investigate pharmacologic methods of limiting excretion of sodium in urine and sweat.
NCT01189344 ↗ Levothyroxine (L-T4) Absorption After Bariatric Surgery Completed University of Sao Paulo N/A 2007-09-01 Intestinal absorption of levothyroxine (LT4) tablets depends on its dissolution in gastric acid secretion, which is reduced after bariatric interventions. Impaired LT4 absorption due to low gastric dissolution has been reported in patients with atrophic or chronic gastritis. The objective of this study is to evaluate the absorption of LT4 tablets in morbidly obese patients before and after Roux-en-Y bariatric surgery.
NCT01866709 ↗ Safety and Efficacy of Sodium Polystyrene Sulfonate in Hyperkalemia Terminated ZS Pharma, Inc. Phase 4 2013-05-01 It is hypothesized that SPS is more effective than placebo control (alternative hypothesis) in lowering i-STAT potassium levels in subjects with i-STAT potassium levels between 5.0 - 6.5 mmol/l versus no difference between SPS and placebo control (null hypothesis).
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for SODIUM POLYSTYRENE SULFONATE

Condition Name

Condition Name for SODIUM POLYSTYRENE SULFONATE
Intervention Trials
Hyperkalemia 3
Acute Hyperkalemia 1
Attention Deficit Hyperactivity Disorder 1
Chronic Kidney Failure 1
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Condition MeSH

Condition MeSH for SODIUM POLYSTYRENE SULFONATE
Intervention Trials
Hyperkalemia 4
Obesity, Morbid 1
Pseudohypoaldosteronism 1
Hyperkinesis 1
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Clinical Trial Locations for SODIUM POLYSTYRENE SULFONATE

Trials by Country

Trials by Country for SODIUM POLYSTYRENE SULFONATE
Location Trials
United States 4
Brazil 1
Canada 1
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Trials by US State

Trials by US State for SODIUM POLYSTYRENE SULFONATE
Location Trials
Florida 2
California 1
New York 1
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Clinical Trial Progress for SODIUM POLYSTYRENE SULFONATE

Clinical Trial Phase

Clinical Trial Phase for SODIUM POLYSTYRENE SULFONATE
Clinical Trial Phase Trials
Phase 4 5
Phase 2 1
N/A 1
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Clinical Trial Status

Clinical Trial Status for SODIUM POLYSTYRENE SULFONATE
Clinical Trial Phase Trials
Completed 5
Recruiting 1
Terminated 1
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Clinical Trial Sponsors for SODIUM POLYSTYRENE SULFONATE

Sponsor Name

Sponsor Name for SODIUM POLYSTYRENE SULFONATE
Sponsor Trials
ZS Pharma, Inc. 1
Department of Pharmacy, Maisonneuve Rosemont Hospital 1
Nephrology Research Axis of Maisonneuve Rosemont Hospital 1
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Sponsor Type

Sponsor Type for SODIUM POLYSTYRENE SULFONATE
Sponsor Trials
Other 9
Industry 2
NIH 1
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