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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04948567
Other study ID # KY20170119-2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 30, 2017
Est. completion date December 1, 2019

Study information

Verified date May 2021
Source Air Force Military Medical University, China
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Adequate bowel preparation is critical for successful colonoscopy and a large volume of PEG was required for bowel preparation in patients undergoing colonoscopy. The investigators conducted a a prospective, randomized, controlled study to compare low dose of oral magnesium sulfate solution with high dose PEG. The investigators found that patients who took low dose of oral magnesium sulfate solution had similar bowel preparation quality to patients who took PEG,but accompanied with fewer adverse events and better tolerance.


Recruitment information / eligibility

Status Completed
Enrollment 1174
Est. completion date December 1, 2019
Est. primary completion date December 1, 2019
Accepts healthy volunteers No
Gender All
Age group 60 Years to 90 Years
Eligibility Inclusion Criteria: - patients who underwent colonoscopy Exclusion Criteria: - known or suspected bowel stricture or obstruction; - history of colorectal surgery; - significant gastroparesis or gastric outlet obstruction; - toxic colitis or megacolon; - severe acute inflammatory bowel disease; - active gastrointestinal bleeding; - suspected or confirmed chronic renal insufficiency and heart illness; - disturbance of electrolytes ; - unable to provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
split-dose of Magnesium Sulfate solution
purgative for bowel preparation
split-dose of PEG
purgative for bowel preparation

Locations

Country Name City State
China Department of Gastroenterology, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese PLA General Hospital, Beijing
China Endoscopic center, Xijing Hospital of Digestive Diseases Xi'an Shanxi

Sponsors (1)

Lead Sponsor Collaborator
Air Force Military Medical University, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The rate of patients with adequate bowel preparation Defined by each segmental BBPS=2 1 year
Secondary The rate of adenoma detection The proportion of participants with at least one adenoma in each group 1 year
Secondary the numbers of patients with adverse events eg. Vomiting, nausea, abdominal pain 1 year
Secondary The cecal intubation rate The rate of colonoscopy reaching the cecum 1 year
Secondary The time of Cecal intubation the time between the intubation and visualization of any of the following anatomic landmarks: ileocecal valve, appendiceal orifice, or terminal ileum during procedure
Secondary the time during Withdrawal phage the inspection time from cecum to rectum during procedure
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