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Last Updated: September 27, 2021

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CLINICAL TRIALS PROFILE FOR BETAINE

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All Clinical Trials for Betaine

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00152815 ↗ Non-alcoholic Fatty Liver Disease (NAFLD) in HIV: The Role of Nutritional Interventions Terminated Ontario HIV Treatment Network Phase 2 2003-10-01 The purpose of this study is to evaluate the effect of a one-year nutritional intervention with either betaine or vitamin E supplementation, or a weight reducing diet and exercise program on liver steatosis and steatohepatitis.
NCT00152815 ↗ Non-alcoholic Fatty Liver Disease (NAFLD) in HIV: The Role of Nutritional Interventions Terminated Johane Allard Phase 2 2003-10-01 The purpose of this study is to evaluate the effect of a one-year nutritional intervention with either betaine or vitamin E supplementation, or a weight reducing diet and exercise program on liver steatosis and steatohepatitis.
NCT00226356 ↗ Natural Supplements for Unipolar Depression Unknown status National Alliance for Research on Schizophrenia and Depression Phase 4 2004-12-01 This study is being conducted to determine the clinical response rate for the regimen of L-methionine, betaine and folate for unipolar depression.
NCT00226356 ↗ Natural Supplements for Unipolar Depression Unknown status Cambridge Health Alliance Phase 4 2004-12-01 This study is being conducted to determine the clinical response rate for the regimen of L-methionine, betaine and folate for unipolar depression.
NCT00283387 ↗ Efficacy of Betaine for Reduction of Urine Oxalate in Patients With Type 1 Primary Hyperoxaluria Completed National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Phase 2 2007-02-01 The aim of this study is to assess the efficacy and safety of betaine in reducing urine oxalate excretion of Type 1 Primary Hyperoxaluria (PHI) patients. Hypothesis: Betaine will effectively reduce urine oxalate excretion in Primary Hyperoxaluria Type I patients.
NCT00283387 ↗ Efficacy of Betaine for Reduction of Urine Oxalate in Patients With Type 1 Primary Hyperoxaluria Completed Orphan Europe Phase 2 2007-02-01 The aim of this study is to assess the efficacy and safety of betaine in reducing urine oxalate excretion of Type 1 Primary Hyperoxaluria (PHI) patients. Hypothesis: Betaine will effectively reduce urine oxalate excretion in Primary Hyperoxaluria Type I patients.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Betaine

Condition Name

Condition Name for Betaine
Intervention Trials
Homocystinuria 3
Healthy 2
Chronic Hepatitis C 2
Retinopathy 1
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Condition MeSH

Condition MeSH for Betaine
Intervention Trials
Homocystinuria 4
Hepatitis C 3
Hepatitis A 3
Hepatitis 3
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Clinical Trial Locations for Betaine

Trials by Country

Trials by Country for Betaine
Location Trials
United States 19
Canada 4
Italy 2
France 1
Serbia 1
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Trials by US State

Trials by US State for Betaine
Location Trials
California 4
Massachusetts 3
North Carolina 2
Nebraska 2
Minnesota 2
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Clinical Trial Progress for Betaine

Clinical Trial Phase

Clinical Trial Phase for Betaine
Clinical Trial Phase Trials
Phase 4 5
Phase 3 2
Phase 2/Phase 3 1
[disabled in preview] 13
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Clinical Trial Status

Clinical Trial Status for Betaine
Clinical Trial Phase Trials
Completed 13
Active, not recruiting 3
Terminated 3
[disabled in preview] 6
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Clinical Trial Sponsors for Betaine

Sponsor Name

Sponsor Name for Betaine
Sponsor Trials
University of California, San Francisco 3
McGill University Health Center 2
Mayo Clinic 2
[disabled in preview] 4
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Sponsor Type

Sponsor Type for Betaine
Sponsor Trials
Other 40
Industry 2
NIH 1
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Serving leading biopharmaceutical companies globally:

Boehringer Ingelheim
McKesson
Express Scripts
Harvard Business School
Medtronic
Colorcon

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