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Initiation of Diet in Esophageal Varices After Ligation (IDEAL) Study

A Comparison of Clear Fluid Diet Initiation Time on Rebleeding Rate and Convenience Level in Liver Cirrhosis Patients Underwent Esophageal Variceal Ligation at Cipto Mangunkusumo Hospital

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04890210
Acronym
IDEAL
Enrollment
130
Registered
2021-05-18
Start date
2021-05-20
Completion date
2021-12-01
Last updated
2021-05-18

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

Conditions

Liver Cirrhosis

Keywords

Esophageal Varices After Ligation, Initiation of Diet, Liver cirrhosis

Brief 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.

Detailed 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.

Interventions

DIETARY_SUPPLEMENTEarly Diet Group

Initiation of clear fluid diet 1 hour after esophageal variceal ligation

DIETARY_SUPPLEMENTLate Diet Group

Initiation of clear fluid diet 6 hours after esophageal variceal ligation

Sponsors

Dr Cipto Mangunkusumo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Liver cirrhosis patients who underwent esophageal variceal ligation

Exclusion criteria

* Hemodynamic instability (shock) * Possible perforation of the esophagus * Esophageal diverticula * Esophageal strictures

Design outcomes

Primary

MeasureTime frameDescription
Early rebleeding event after esophageal variceal ligationThis outcome (early rebleeding) will be assessed within 5 days after esophageal variceal ligationEarly rebleeding event is hematemesis, melena and/or hematochezia that occurs within 5 days (120 hours) after esophageal variceal ligation

Secondary

MeasureTime frameDescription
Late rebleeding event after esophageal variceal ligationThis outcome (late rebleeding) will be assessed between over than 5 days until 28 days after esophageal variceal ligationLate rebleeding event is hematemesis, melena and/or hematochezia that occurs between over than 5 days until 28 days after esophageal variceal ligation

Other

MeasureTime frameDescription
Patient's convenience level regarding initiation of diet after esophageal variceal ligationPatient's convenience will be measured 30 minutes after the patient finished the 1st clear fluid dietPatient's convenience is subjectively measured using Visual Analogue Scale (VAS) 0-10 cm with 0 is very unconvenient and 10 is very convenient

Contacts

Primary ContactRabbinu R Pribadi, MD
rabbinurangga@gmail.com+6285885382231
Backup ContactMegawati Ananda H Putri, MD
megawatianandadr@gmail.com+6281294052702

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026