A study to compare the effect on tolerance with or without medication (Glycopyrrolate) in patients undergoing upper gastrointestinal endoscopy without sedatio

Not Applicable

• Registration Number: CTRI/2020/07/026786
• Lead Sponsor: Jawaharlal Institute of Postgraduate Medical Education and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients aged 18-60 years, undergoing unsedated diagnostic upper GI endoscopy

Exclusion Criteria

a.History of glaucoma

b.Known cardio respiratory disease

c.Persons with chronic constipation

d.History of obstructive urinary disorders

e.Prior gastrectomy

f.Persons taking anti-anxiety medications

g.Pregnancy

h.History of prior upper GI endoscopy

i.Active upper respiratory infection

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.To assess effect of premedication with glycopyrrolate on the level of patient tolerance during unsedated upper GI endoscopyTimepoint: 60 minutes

Secondary Outcome Measures

Name	Time	Method
1.To study the cardio - respiratory fluctuations during unsedated upper GI endoscopy <br/ ><br> <br/ ><br>2.To study the effect of premedication on the duration of unsedated upper GI endoscopy <br/ ><br> <br/ ><br>3.To assess the number of failed endoscope intubations and incomplete endoscopies <br/ ><br> <br/ ><br>4.To calculate the Endoscopistâ??s assessment score after the unsedated upper GI endoscopy <br/ ><br>Timepoint: 60 minutes