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Last Updated: December 13, 2024

CLINICAL TRIALS PROFILE FOR LACTULOSE


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All Clinical Trials for Lactulose

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00004796 ↗ Phase II Study of Lactulose and Circadian Rhythms in Patients With Cirrhosis Completed Northwestern University Phase 2 1994-11-01 OBJECTIVES: I. Assess the effect of lactulose on the circadian rhythm of plasma melatonin in patients with subclinical hepatic encephalopathy. II. Assess the intrasubject variability of circadian melatonin levels and neuropsychological tests. III. Assess which elements of the neuropsychological test battery show the response to lactulose.
NCT00004796 ↗ Phase II Study of Lactulose and Circadian Rhythms in Patients With Cirrhosis Completed National Center for Research Resources (NCRR) Phase 2 1994-11-01 OBJECTIVES: I. Assess the effect of lactulose on the circadian rhythm of plasma melatonin in patients with subclinical hepatic encephalopathy. II. Assess the intrasubject variability of circadian melatonin levels and neuropsychological tests. III. Assess which elements of the neuropsychological test battery show the response to lactulose.
NCT00133406 ↗ Long-term Impact and Intervention for Diarrhea in Brazil Unknown status National Institute of Allergy and Infectious Diseases (NIAID) Phase 3 2006-06-01 The primary objectives of this study are to determine the effect of 1 year supplementation of Vitamin A, Zinc, and Vitamin A plus Zinc compared to placebo on the Height for Age Z Score (HAZ) and the number of episodes of diarrhea and number of days of diarrhea at one year in children living in a Brazilian slum. Study participants will include 280 children ages 2 months to 8 years old, with a Height for Age Z score (HAZ) less than median for the Parque Universitario community, living in Brazilian favela. There is also a sub study to determine if ten days of glutamine delivered as an oral bolus improves the health of the digestive system.
NCT00133406 ↗ Long-term Impact and Intervention for Diarrhea in Brazil Unknown status University of Virginia Phase 3 2006-06-01 The primary objectives of this study are to determine the effect of 1 year supplementation of Vitamin A, Zinc, and Vitamin A plus Zinc compared to placebo on the Height for Age Z Score (HAZ) and the number of episodes of diarrhea and number of days of diarrhea at one year in children living in a Brazilian slum. Study participants will include 280 children ages 2 months to 8 years old, with a Height for Age Z score (HAZ) less than median for the Parque Universitario community, living in Brazilian favela. There is also a sub study to determine if ten days of glutamine delivered as an oral bolus improves the health of the digestive system.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Lactulose

Condition Name

Condition Name for Lactulose
Intervention Trials
Hepatic Encephalopathy 40
Constipation 13
Liver Cirrhosis 13
Cirrhosis 10
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Condition MeSH

Condition MeSH for Lactulose
Intervention Trials
Hepatic Encephalopathy 51
Brain Diseases 50
Liver Cirrhosis 25
Fibrosis 23
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Clinical Trial Locations for Lactulose

Trials by Country

Trials by Country for Lactulose
Location Trials
United States 141
China 23
India 19
United Kingdom 8
Egypt 6
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Trials by US State

Trials by US State for Lactulose
Location Trials
New York 11
California 10
Virginia 8
Texas 7
Massachusetts 6
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Clinical Trial Progress for Lactulose

Clinical Trial Phase

Clinical Trial Phase for Lactulose
Clinical Trial Phase Trials
Phase 4 36
Phase 3 19
Phase 2/Phase 3 10
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Clinical Trial Status

Clinical Trial Status for Lactulose
Clinical Trial Phase Trials
Completed 71
Unknown status 24
Recruiting 24
[disabled in preview] 10
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Clinical Trial Sponsors for Lactulose

Sponsor Name

Sponsor Name for Lactulose
Sponsor Trials
Valeant Pharmaceuticals International, Inc. 9
Bausch Health Americas, Inc. 8
Institute of Liver and Biliary Sciences, India 7
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Sponsor Type

Sponsor Type for Lactulose
Sponsor Trials
Other 214
Industry 56
NIH 8
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