Clinical Trials Directory

Trials / Completed

CompletedNCT04682860

Management of Abdominal Pain in Acute Gastroenteritis Patients With Hyoscine Butylbromide

Management of Abdominal Pain in Acute Gastroenteritis Patients With Hyoscine Butylbromide: Randomized Double Blind Placebo Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Ankara City Hospital Bilkent · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

One of the most common complaints of admission to the emergency room is gastroenteritis. One of the most common complaints in acute gastroenteritis is abdominal pain. The aim of our study is to investigate whether hyoscine butylbromide used within the indication has an effect on abdominal pain due to acute gastroenteritis. The main purpose of our study is to reduce the pain of the patient at 30th and 60th minutes compared to 0th minute.

Conditions

Interventions

TypeNameDescription
DRUGHyoscine N ButylbromideHyoscine N butylbromide injection for the treatment of abdominal pain in acute gastroenteritis
OTHERPlacebo2 ml of normal saline injection as placebo

Timeline

Start date
2021-09-08
Primary completion
2021-12-03
Completion
2022-01-03
First posted
2020-12-24
Last updated
2022-01-04

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04682860. Inclusion in this directory is not an endorsement.