Ignite Creation Date:
2025-12-25 @ 3:07 AM
Ignite Modification Date:
2025-12-26 @ 1:47 AM
Study NCT ID:
NCT03760133
Status:
COMPLETED
Last Update Posted:
2020-02-20
First Post:
2018-11-25
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
The Change of Gut Microbiota After Bowel Preparation and the Effect of Probiotics
Sponsor:
Kosin University Gospel Hospital
Organization:
Study Overview
Official Title:
The Change of Gut Microbiota After Bowel Preparation and the Effect of Probiotics: Randomized Controlled, Open-label Trial
Status:
COMPLETED
Status Verified Date:
2020-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to investigate the relationship between the change of intestinal bacterial flora and the recovery, and the incidence of symptoms such as abdominal discomfort after colonoscopy. And the investigators will also analyze the effects of probiotics on the degree of change, recovery, and symptom development in intestinal flora.
Detailed Description:
The investigators divided two groups. (total number = 100 subjects)
1. with probiotics group - 50 subjects
* Participants included in this group will be taken probiotics for 1 month after bowel preparation for colonoscopy.
2. without probiotics group - 50 subjects
* Participants included in this group will not be taken probiotics for 1 month after bowel preparation for colonoscopy.
1. with probiotics group - 50 subjects
* Participants included in this group will be taken probiotics for 1 month after bowel preparation for colonoscopy.
2. without probiotics group - 50 subjects
* Participants included in this group will not be taken probiotics for 1 month after bowel preparation for colonoscopy.
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?: