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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05542810
Other study ID # Guangzhou Medical University
Secondary ID
Status Not yet recruiting
Phase Early Phase 1
First received
Last updated
Start date January 1, 2023
Est. completion date December 31, 2023

Study information

Verified date September 2022
Source Guangzhou Medical University
Contact Gan Huoye
Phone 13927688350
Email gzyghy04@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, 200 patients were enrolled from 2023.1.1 to 2023.12.31, and were randomly divided into intervention and control groups. The intervention group compared the effectiveness of intestinal preparation in the two groups with sports drinks as a polyethylene glycol solvent and water as a polyethylene glycol solvent in the intervention group, and compared adverse reactions, acceptability of solution taste, time of oral laxatives, willingness to repeat the same intestinal preparation or the willingness to recommend the same intestinal preparation to others.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: Hospitalized patients with gastrointestinal disorders Age 18 to 25 years Exclusion Criteria: Those who refuse to drink sports drinks Hypersensitivity to polyethylene glycol pregnant women, patients with suspected intestinal obstruction patients at risk of aspiration or with severe systemic or poorly controlled chronic disease patients with acute or severe disease and coagulation disorders patients with diabetes mellitus patients with a history of abdominal surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Combination Product:
Use sports drinks as polyethylene glycol solvents
Using sports drinks as a polyethylene glycol solvent and water as a polyethylene glycol solvent in the control group, the effectiveness of intestinal preparation in the two groups was compared, and the adverse reactions, the acceptability of the solution taste, the timing of oral laxatives, and the willingness to repeat the same intestinal preparation or the willingness to recommend the same intestinal preparation to others were compared.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
GanHuoye

Outcome

Type Measure Description Time frame Safety issue
Primary A prospective randomized trial to compare the effectiveness of sports drink and water as a solvent in polyethylene glycol for colonoscopy After drinking, a questionnaire was used to compare the adverse reactions, acceptance, preparation time, and differences in the patient's willingness to prepare again or to recommend the same intestinal preparation method to others, and the results were expressed numerically. 1year
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