CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 110 enrolled
Drug / intervention
placebo +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01948921
NCT01948921N/ACompleted

Meperidine as the Single Sedative Agent for Patients Expected to Have Poor Tolerance During Diagnostic Esophagogastroduodenoscopy.

Dalin Tzu Chi General Hospital·interventional·Posted Sep 24, 2013·Updated Mar 20, 2017

In Brief

A clinical study evaluating placebo and Meperidine for Patients Undergoing Diagnostic EGD. Completed, enrolled 110 participants across 1 site.

Detailed Summary

Our pilot results showed that meperidine reduce patient discomfort during EGD (esophagogastroduodenoscopy). But many patients can tolerate EGD well without any sedative agents. So the investigators target the use of meperidine on patients expected to have poor tolerance in this study, which includ young females with high anxiety level and patients with prior poor tolerance. The investigators test the hypothesis that meperidine improves tolerance and alleviates discomfort for patients expected to have poor tolerance during diagnostic EGD.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesTaiwan
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedSep 24, 2013
Enrollment StartSep 1, 2013
Primary CompletionMar 1, 2017
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 12.8 years ago

Interventions

placebodrug

Meperidinedrug