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DILI is an underdiagnosed and under appreciated causal or contributing factor to liver injury. DILI can mimics features of the entire spectrum of acute and chronic liver disease.
Asia-Pacifc region is characterized by two unique features; the high prevalence of tuberculosis (TB) in the population and the ubiquitous use of traditional and complimentary medicines.Current definition of Hy's law presents significant difficulties when dealing with patients with preexisting CLD in clinical trials. Hallmark of the hepatic manifestation in these patients is hyperbilirubinemia and coagulopathy rather than ALT elevation.
Study Design Single-center, non-blinded, parallel group, randomized controlled trial. Allocation ratio between two groups: 1:1.
Study population: Adults aged 18-75 years with previously known or unknown underlying CLD Diagnosis of DILI-based causality of assessment by RECAM. Severe DILI with bilirubin > 12mg/dl or INR>2, S.Bili >5 mg/dl Consent to participate in the study (based on biopsy, imaging or clinical criteria).
Study design: RCT Study period: 1 year Sample size: 96 Intervention: Patients after screening for all exclusion criteria will be randomized into either the standard treatment group or the plasma exchange group.
Monitoring and assessment: All patients would undergo vital and baseline parameter screening before randomization. Based on randomization they will receive either steroid or plasma exchange followed by steroid.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PLEX with SMT | Experimental | High Volume Plex with minimum 3 sessions on alternate days along with Standard treatment. |
|
| Standard Medical Treatment | Active Comparator | Standard treatment. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| High volume Plasma Exchange | Biological | High volume Plasma Exchange with minimum 3 sessions on alternate days |
|
| Measure | Description | Time Frame |
|---|---|---|
| Liver Transplant free survival at the end of 30 days between two groups. | 30 days |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in arterial lactate levels, on lactate clearance at 0, 3, 5 days | 0, 3, 5 days | |
| Reduction in von Willebrand factor levels, endothelial function, and coagulopathy at 0 and 30 day. | 0 and 30 day. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dr Khushboo Yadav, MD | Contact | 01146300000 | ky29277@gmail.com | |
| Dr Shasthry SM, DM | Contact | 01146300000 | shasthry@gmail.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institute of Liver & Biliary Sciences (ILBS) | New Delhi | National Capital Territory of Delhi | 110070 | India |
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| Standard Medical Treatment | Other | Standard Medical Treatment includes stopping the offending drug,nutrition,injection NAC,Tablet UDCA,steroid in DILI AIH |
|
| Changes in the inflammatory milieu, IL6, IL10, and TNF alpha at 0 and 30 day. | 0 and 30 day. |
| Change in liver-related decompensation events (ascites, HE, variceal bleed) at 0, 3, 5,30, and 90 days. | 0, 3, 5,30, and 90 days. |
| Change in serum bilirubin and bile acids clearance at 0, 3, 5,30 and 90 days. | 0, 3, 5,30 and 90 days. |
| ID | Term |
|---|---|
| D056486 | Chemical and Drug Induced Liver Injury |
| ID | Term |
|---|---|
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D064420 | Drug-Related Side Effects and Adverse Reactions |
| D064419 | Chemically-Induced Disorders |
| D011041 | Poisoning |
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