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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00905996
Other study ID # SRM04
Secondary ID
Status Completed
Phase N/A
First received May 19, 2009
Last updated May 20, 2009
Start date August 2006
Est. completion date January 2009

Study information

Verified date May 2009
Source Govind Ballabh Pant Hospital
Contact n/a
Is FDA regulated No
Health authority India: Ministry of Health
Study type Interventional

Clinical Trial Summary

In patients who have never bled from gastric varix (GOV2 and IGV1), cyanoacrylate injection will be better than both beta-blocker therapy and no treatment in prevention of gastric variceal bleed. The investigators conducted a randomized controlled trial in patients with gastric varix (GOV2 and IGV1) who never bled before, to study the efficacy of treatment with cyanoacrylate injection versus beta-blocker versus no treatment in prevention of first bleed from gastric varices.


Description:

Patients are followed up every 3 months or at the time of end point or complications.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender Both
Age group 12 Years to 75 Years
Eligibility Inclusion Criteria:

- Patients with GOV2 with eradicated esophageal varix or IGV1, who had never bled from gastric varix were included.

Exclusion Criteria:

- Only esophageal varix, GOV1 with GOV2, acute bleed or past history of bleed from gastric varix, contraindications to beta-blocker therapy and cyanoacrylate injection.

- Prior injection of cyanoacrylate or sclerotherapy or variceal ligation or transjugular intrahepatic portosystemic shunt or balloon-occluded retrograde transvenous obliteration or balloon-occluded endoscopic injection sclerotherapy of gastric varix for prevention of bleeding from GV

- Patients already on beta-blocker or nitrates

- Undetermined origin of bleeding from esophageal varix or gastric varix

- Hepatic encephalopathy grade III/IV

- Hepatorenal syndrome

- Hepatocellular carcinoma

- Presence of deep jaundice (serum bilirubin > 10 mg/dl)

- Uremia

- Cerebrovascular accident

- Cardiorespiratory failure

- Pregnancy and patients not giving informed consent for endoscopic procedures

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Procedure:
Endoscopic cyanoacrylate injection
Endoscopic cyanoacrylate injection in gastric varix
Drug:
Beta-blocker (propranolol)


Locations

Country Name City State
India Shiv K Sarin New Delhi Delhi

Sponsors (1)

Lead Sponsor Collaborator
Govind Ballabh Pant Hospital

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bleeding from gastric varix or death Within 2 years No
Secondary Increase or decrease in the size of gastric varices, appearance of new esophageal varices and appearance or worsening of portal hypertensive gastropathy (PGP), complications Within 2 years Yes
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