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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02119000
Other study ID # GEN 13-148
Secondary ID GEN 13-148
Status Terminated
Phase Phase 4
First received
Last updated
Start date August 2015
Est. completion date January 2020

Study information

Verified date February 2021
Source McGill University Health Centre/Research Institute of the McGill University Health Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Bowel preparation is a crucial step prior to colonoscopy to help with the optimal assessment of the colonic mucosa. Inadequate bowel preparation increases the length of the procedure, and is associated with decreased lesional detection rates. The ideal bowel preparation formulation should be able to completely clean the bowel, without leaving solid or liquid residues, and without modifying the mucosal appearance. Bowel preparation may be administered in hospitalised patients or in the ER. Patients have less control on their environment and the intake of the bowel preparation. For example, there may be a delay in pharmacy delivery or inadequate supervision by the treating personnel. Hospitalised patients have more comorbidities, are usually less autonomous and mobile - both can add to the barriers leading to an adequate bowel preparation. Multiple studies have identified hospitalization status as an independent risk factor for poor bowel preparation. The objective of this study is to access which bowel preparation regimen, between PEG 3350 with electrolytes 2L the day before and 2L the day of the colonoscopy vs bisacodyl + PEG 3350 with electrolytes 1L the day before and 1L the day of the colonoscopy, results in the cleanest bowel preparation in hospitalised patients.


Recruitment information / eligibility

Status Terminated
Enrollment 82
Est. completion date January 2020
Est. primary completion date January 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria - 18 years or older - Be able to comprehend the trial and provide written informed consent in French or English, or a close relative with power of attorney - Have a recognised indication for full colonoscopy after evaluation by a gastroenterologist or surgeon - Be hospitalized or in the ED of a participating hospital center. - Need to receive a bowel preparation during hospitalization or the ED stay. - Be able to complete the follow-up patient response form in French or English Exclusion Criteria: - Patient refusal - A suspected or diagnosed bowel obstruction - A toxic megacolon - Ileus - Decompensated heart failure - Severe acute renal failure - Severe electrolyte imbalance - Previous bowel preparation in the last 7 days - Pregnancy - Time of randomization before 9h00 or after 22h00

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
PEG/electrolytes 2L/2L split dose
Polyethylene glycol 17gm X 4 At 18h00 the day prior the colonoscopy, dilute 2 sachets in 2 L of water and drink 240 mL every 10 minutes On the day of the procedure, 4-5 hours prior the colonoscopy, dilute 2 sachets in 2 L of water and drink 240 mL every 10 minutes
Bisacodyl 15 mg and PEG/electrolytes 1L/1L split dose
Bisacodyl 15 mg x 3 At 14h00 the day prior the endoscopic procedure: take 3 tablets of Bisacodyl ER (15 mg) orally then 5 hr later: PEG/electrolytes 1L/1L Polyethylene glycol 17gm Dilute one sachet of Polyethylene glycol 17gm in 1 L of water Start drinking at around 19h00 the night prior the colonoscopy Drink 240 ml every 10 minutes The day of the colonoscopy. At (4 hrs prior the procedure). Dilute on sachet of PEG and drink 240 ml every 10 minutes

Locations

Country Name City State
Canada McGill University Health Centre Montreal Quebec
Canada Centre hospitalier universitaire de Sherbrooke Sherbrooke Quebec

Sponsors (1)

Lead Sponsor Collaborator
McGill University Health Centre/Research Institute of the McGill University Health Centre

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy Which bowel preparation regimen, between PEG 3350 with electrolytes 2L the day before and 2L the day of the colonoscopy vs bisacodyl + PEG 3350 with electrolytes 1L the day before and 1L the day of the colonoscopy, results in the cleanest bowel preparation in hospitalised patients. following colonoscopy
Secondary Tolerability A questionnaire will be used to assess which is the most tolerable and acceptable to patients between the two bowel preparation regimens Before colonoscopy
Secondary Clinical quality standards Does the bowel preparation given prior to in-hospital colonoscopy result in an excellent or good preparation rate that falls within the required clinical quality standards? After colonoscopy
Secondary Cecal/ileal intubation rate What is the cecal/ileal intubation rate for colonoscopies performed in hospitalized patients? Following colonoscopy
Secondary Polyp detection rate What is the polyp detection rate for colonoscopies performed in hospitalized patients? Following colonosopy
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