Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06153082

Rotational Thromboelastometry [ROTEM] vs Thromboelastography [TEG] Guided Blood Component Use in Patients With Cirrhosis of Liver With Non-variceal Bleeding.

Led by Institute of Liver and Biliary Sciences, India · Updated on 2024-08-07

80

Participants Needed

1

Research Sites

54 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is aim to compare ROTEM and TEG guided coagulopathy correction in cirrhosis with non- variceal bleed.There are no other study in literature to compare this two group in cirrhosis with non-variceal bleed.This study will also assess the volume of blood product transfused with this two groups and it will compare among two groups.This will lessen the blood product transfusion and risk of transfusion relatedated complication.

CONDITIONS

Official Title

Rotational Thromboelastometry [ROTEM] vs Thromboelastography [TEG] Guided Blood Component Use in Patients With Cirrhosis of Liver With Non-variceal Bleeding.

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with cirrhosis of any cause
  • Age between 18 and 80 years
  • Presenting with nonvariceal upper gastrointestinal bleeding confirmed by endoscopy
  • Significant coagulopathy with INR > 1.8 and/or platelet count < 50 � 10^9/L
Not Eligible

You will not qualify if you...

  • Variceal bleeding
  • Bleeding from post-variceal ligation ulcers
  • History of blood clots in veins or arteries
  • Use of anti-platelet or anticoagulant therapy within 7 days before enrollment
  • Pregnancy
  • Significant heart or lung diseases

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dr Saurav Paul

New Delhi, National Capital Territory of Delhi, India, 110070

Actively Recruiting

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Research Team

D

Dr Saurav Paul, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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