Seven Day Versus Fourteen-day Corticosteroid in Patients With Severe Alcohol -Associated Hepatitis- A Double Blind Randomized Controlled Trail (STASH II)

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Alcohol-associated hepatitis (AAH) is one of the most severe manifestations of the spectrum of alcohol related liver disease (ARLD), with high morbidity and mortality. Currently, corticosteroids are the standard of care for patients with severe AAH, but no consensus exists on the dosing schedule of steroids. The investigators have recently demonstrated that tapering prednisolone over 4 weeks reduces the risk of infections at day 90. However, the investigators wanted to test whether the reduction in the duration of therapy would provide a similar benefit as tapering the dose of prednisolone. Therefore, the investigators planned to assess the impact of a shorter duration of prednisolone on outcomes, including the incidence of infections, survival and adverse events. One group will receive 7 days of prednisolone followed by a placebo for the next seven days, and the other group will receive 40 mg of prednisolone for 14 days. Prednisolone will be stopped in case of non-response and/or adverse events to the drug. All infections will be diagnosed by an ID specialist who is blind to the allocated group.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Patients with AAH aged between 18 and 80 years with a MELD score \>21 and/or mDF \>32 will be included.

• Patients with infection at baseline will be included if they have controlled infection defined as afebrile for at least 48 hours, sterile cultures and procalcitonin \< 1 ng/ml.

Locations
Other Locations
India
AIG
RECRUITING
Hyderabad
AIG Hospitals
RECRUITING
Hyderabad
Contact Information
Primary
ANAND KULKARNI V DR. ANAND V KULKARNI, SENIOR CONSULTANT
anandvk90@gmail.com
04042444222
Backup
Sridevi prasanna daparti, DR
deviprasanna9804@gmail.com
04042444222
Time Frame
Start Date: 2025-04-07
Estimated Completion Date: 2026-04-08
Participants
Target number of participants: 146
Treatments
Active_comparator: Prednisolone dose of 40mg/day for 7 days
Participants satisfying the inclusion criteria will be randomly allocated. Participants in Group A will receive prednisolone dose of 40 mg/day for 7 days after which the participants will recieve seven days of prednisolone 40 mg/day for next 7 days provided they had responded on day 7 based on Lille score
Active_comparator: Prednisolone dose of 40mg/day for 14 days
Participants satisfying the inclusion criteria will be randomly allocated. Participants in Group B will receive prednisolone dose of 40 mg/day for 14 days only if they respond to on day 7 based on Lille score
Related Therapeutic Areas
Sponsors
Collaborators: Apollo Gleneagles Hospitals, Kolkata, Kalinga Institute of Medical Sciences, Bhubaneswar, Mahatma Gandhi Medical College, Post Graduate Institute of Medical Education and Research, Chandigarh
Leads: Asian Institute of Gastroenterology, India

This content was sourced from clinicaltrials.gov