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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02161653
Other study ID # DI/10/107/3/43
Secondary ID
Status Completed
Phase Phase 4
First received June 10, 2014
Last updated November 8, 2014
Start date April 2010
Est. completion date September 2014

Study information

Verified date November 2014
Source Hospital General de Mexico
Contact n/a
Is FDA regulated No
Health authority Mexico: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether metadoxine is effective for improve survival and reduced oxidative stress in patients with severe alcoholic hepatitis.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients with clinical and biochemical criteria for severe alcoholic hepatitis: Total bilirubin greater than 5 mg/dl in absence of biliary tract obstruction evidenced by ultrasound, history of chronic alcohol intake, leukocytosis, neutrophilia, elevation of transaminases with an aspartate aminotransferase / alanine aminotransferase ratio equal or greater than 2, discriminant function greater than 32.

Exclusion Criteria:

- Diabetes, chronic kidney disease, hepatitis C, hepatitis B and or human immunodeficiency virus infection, asthma or history of atopy or allergic reactions, therapy in the previous two years with steroids, pentoxifylline, metadoxine, S-adenosyl L- methionine, antioxidants or multivitamins.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
Prednisone plus Metadoxine

Pentoxifylline plus Metadoxine


Locations

Country Name City State
Mexico Hospital General de Mexico Mexico City D.f.

Sponsors (1)

Lead Sponsor Collaborator
Hospital General de Mexico

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30 day-survival 30 days No
Primary Malondialdehyde serum levels 14 and 30 days No
Secondary 3 month-survival 3 months No
Secondary 6 month-survival 6 months No
See also
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Not yet recruiting NCT06155760 - Role of Extended Low Dose Prednisolone in Achieving Clinical and Biochemical Remission in Steroid Responsive Severe Alcoholic Hepatitis N/A
Completed NCT02808663 - Assessment of the Predictive Value of Fecal Calprotectin for the Outcome of Severe Alcoholic Hepatitis N/A
Completed NCT01820208 - Efficacy of G-CSF in the Management of Steroid Non-responsive Severe Alcoholic Hepatitis N/A
Withdrawn NCT03087968 - Evaluation of HepQuant SHUNT to Assess Liver Disease; Substudy Within GS-US-416-2124 Early Phase 1
Not yet recruiting NCT02485106 - Rifaximin Use in Severe Alcoholic Hepatitis Phase 3
Recruiting NCT03827772 - Fecal Microbiota Transplantation in Severe Alcoholic Hepatitis- Assessment of Impact on Prognosis and Short-term Outcome N/A
Completed NCT01801332 - Intensive Enteral Nutrition and Acute Alcoholic Hepatitis N/A
Recruiting NCT04103840 - Invasive Fungal Infections in Severe Alcohol-associated Hepatitis
Active, not recruiting NCT03091010 - A Comparison of Fecal Microbiota Transplantation and Steroid Therapy in Patients With Severe Alcoholic Hepatitis. N/A