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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04890210
Other study ID # DCiptoMGH Indonesia
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 20, 2021
Est. completion date December 1, 2021

Study information

Verified date May 2021
Source Dr Cipto Mangunkusumo General Hospital
Contact Rabbinu R Pribadi, MD
Phone +6285885382231
Email rabbinurangga@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

1. Objective The purpose of this study is to evaluate whether there is a significant difference of early rebleeding rate (within the first 5 days after esophageal variceal ligation), late rebleeding rate (more than 5 days until 28 days after esophageal variceal ligation), and convenience level between cirrhotic patients in early diet group versus late diet group. 2. Method This study is a single blind randomised clinical trial. Subjects will be selected based on inclusion and exclusion criteria, then the subjects will be randomly divided into 2 groups, the early diet group (clear fluid diet is initiated 1 hour after esophageal variceal ligation) and the late diet group (clear fluid diet is initiated 6 hours after esophageal variceal ligation). The intervention arm is the early diet group, while the control arm is the late diet group. The primary outcome is the early rebleeding rate. The secondary outcomes are late rebleeding rate and patient's convenience level which will be measured using Visual Analogue Scale (VAS). 3. Expected result The expected result is there will be no difference in early bleeding rate, late bleeding rate, and convenience level between early diet group versus late diet group.


Description:

This study is a single blind randomised controlled trial (RCT) that will be conducted at gastrointestinal endoscopy center division of gastroenterology, integrated procedure room division of hepatobiliary, department of internal medicine, gastroenterology clinic, hepatobiliary clinic, internal medicine ward, high care unit (HCU) and intensive care unit (ICU) Cipto Mangunkusumo Hospital - Faculty of Medicine Universitas Indonesia from May 20, 2021-November 1, 2021. The proposed number of subjects are 130 patients. Interventions will be given in the form of early clear fluid diet initiation compared to active comparator in the form of late clear fluid diet initiation in eligible liver cirrhosis patients who undergo esophageal variceal ligation (EVL) at Cipto Mangunkusumo Hospital. In early diet group diet, the 100 ml of clear fluid will be initiated at 1 hour after EVL followed by standard protocol (clear fluid, soft porridge, porridge, soft rice, regular rice) explained in the arms and intervention column below. In late diet group, the 100 ml of clear fluid will be initiated at 6 hours after EVL, followed by standard protocol (clear fluid, soft porridge, porridge, soft rice, regular rice) explained in the arms and intervention column below. Other routine and standardised drugs for liver cirrhosis patients will still be given. Statistical analysis will use Chi square test with alternative Fisher test for categorical dependent variables and independent T-test with alternative Mann-Whitney test for two group numerical dependent variables.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 130
Est. completion date December 1, 2021
Est. primary completion date November 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Liver cirrhosis patients who underwent esophageal variceal ligation Exclusion Criteria: - Hemodynamic instability (shock) - Possible perforation of the esophagus - Esophageal diverticula - Esophageal strictures

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Early Diet Group
Initiation of clear fluid diet 1 hour after esophageal variceal ligation
Late Diet Group
Initiation of clear fluid diet 6 hours after esophageal variceal ligation

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Dr Cipto Mangunkusumo General Hospital

Outcome

Type Measure Description Time frame Safety issue
Other Patient's convenience level regarding initiation of diet after esophageal variceal ligation Patient's convenience is subjectively measured using Visual Analogue Scale (VAS) 0-10 cm with 0 is very unconvenient and 10 is very convenient Patient's convenience will be measured 30 minutes after the patient finished the 1st clear fluid diet
Primary Early rebleeding event after esophageal variceal ligation Early rebleeding event is hematemesis, melena and/or hematochezia that occurs within 5 days (120 hours) after esophageal variceal ligation This outcome (early rebleeding) will be assessed within 5 days after esophageal variceal ligation
Secondary Late rebleeding event after esophageal variceal ligation Late rebleeding event is hematemesis, melena and/or hematochezia that occurs between over than 5 days until 28 days after esophageal variceal ligation This outcome (late rebleeding) will be assessed between over than 5 days until 28 days after esophageal variceal ligation
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