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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02646202
Other study ID # Scleroligation
Secondary ID
Status Recruiting
Phase Phase 3
First received January 1, 2016
Last updated December 22, 2017
Start date January 2015
Est. completion date December 2021

Study information

Verified date December 2017
Source Tanta University
Contact Sherief M. Abd-Elsalam, Consultant
Phone 00201095159522
Email sherif_tropical@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Gastric varices occur in 5-33% of patients with portal hypertension. Concomitant gastro esophageal varices are the most common type. Both endoscopic sclerotherapy and band ligation are very effective in controlling acute esophageal varices bleeding and preventing rebleeding.


Description:

Evaluation of a new scleroligation technique for management of bleeding gastro-esophageal varices regarding efficacy, complications, variceal recurrence, and survival.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- cirrhotic patients presenting with an acute or recent episode of gastro-esophageal variceal bleeding.

Exclusion Criteria:

- Patients were excluded if they had malignancy of any origin.

- Any terminal illness, such as heart failure, uremia, or chronic pulmonary diseases.

- Other potential causes of GIT bleeding.

- Patients with previous endoscopic or surgical intervention for varices were also excluded.

Study Design


Intervention

Procedure:
Sclerotherapy
Injection of varices
Band ligation
endoscopic banding of varices
Scleroligation
intra variceal endoscopic sclerotherapy combined with band ligation.

Locations

Country Name City State
Egypt Tropical medicine dept.-Tanta university hospital Tanta

Sponsors (2)

Lead Sponsor Collaborator
Sherief Abd-Elsalam Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of sessions to complete variceal obliteration 1 year
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