Clinical Trials Directory

Trials / Completed

CompletedNCT01948921

Meperidine for Patients Expected to Have Poor Tolerance During Diagnostic Esophagogastroduodenoscopy.

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
110 (actual)
Sponsor
Dalin Tzu Chi General Hospital · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGplacebo
DRUGMeperidine

Timeline

Start date
2013-09-01
Primary completion
2017-03-01
Completion
2017-03-01
First posted
2013-09-24
Last updated
2017-03-20

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT01948921. Inclusion in this directory is not an endorsement.