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Comparison of a drug (Octreotide) which reduces bleeding by decreasing blood pressure with a control agent in stopping blood vomiting in patients with alcoholic liver disease after band occlusion of the bleeding vessels.

Comparison of octreotide vs placebo in bleeding esophageal varices in cirrhotic patients after endoscopic banding: A prospective double blinded randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012860
Enrollment
270
Registered
2018-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- All the patients presenting with bleeding esophageal varices due to cirrhosis presenting to the emergency department during the study period.

Interventions

Intervention1: Octreotide: Octreotide, a somatostatin analogue is a vasoactive amine used in decreasing portal hypertension. In case of active upper gastrointestinal bleeding due to esophageal varices

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: All patients presenting with bleeding esophageal varices due to cirrhosis to the emergency department during the study period

Exclusion criteria

Exclusion criteria: (1) Non cirrhotic patients with portal hypertension. (2) Extremes of ages; 60 years. (3) Patients in hepatic encephalopathy grades 3 and 4. (4) Patients with source of bleeding in addition to or other than esophageal varices which includes gastritis, ulcers, ectasias, gastric varices, portal gastropathy. (5) Patients already on vasoactive drugs for current episode of bleeding. (6)Patients already received endoscopic ligation for the current episode elsewhere. (7) Patients requiring Sengstaken Blakemore Tube(SBT) insertion. (8)Any history of past surgeries for portal hypertension. (9)Patients associated with severe cardiopulmonary disease or malignancy. (10)Patients not willing to participate in the study.

Design outcomes

Primary

MeasureTime frame
Re-bleeding rates in both the Octreotide and the Placebo groups are compared.Timepoint: Re-bleeding rates are compared in both the groups at the end of three days.

Secondary

MeasureTime frame
not applicableTimepoint: not applicable

Countries

India

Contacts

Public ContactRaj Kumar N

JIPMER

raj.jipmer@gmail.com9443292979

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026