Viewing Study NCT06569966



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06569966
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-20

Brief Title: The Effects of Colorectal Prehabilitation Via Reinfusion or Retention Enema of Ileal Contents Filtrate on the Defecation Functions for the LAR Patients With Ileostomy Before Stoma Closure
Sponsor: None
Organization: None

Study Overview

Official Title: The Effects of Colorectal Prehabilitation Via Reinfusion or Retention Enema of Ileal Contents Filtrate on the Defecation Functions for the LAR Patients With Ileostomy Before Stoma Closure A Single Center Prospective Randomized Controlled Study
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study was a single-center RCT study to compare the effect of preoperative prehabilitation treatment of ileostomy contents filtrate reinfusion through distal ileocolon or retention of enema colon with that of traditional treatment in patients with bowel function after stoma closure
Detailed Description: The patients in the experimental group collected the contents of the ileostomyand placed in a wide mouth container mixed with 500mL normal temperature saline and placed in a funnel with double layer medical gauze The filtrate of the ileal contents was collected and placed into an enema for use The catheter was placed into the ileal output end of the ostomy through anterograde enema or transanal retention enema and slowly infused for 15-20 minutes 2-3 times a day for 4 weeks The adverse reactions such as abdominal pain abdominal distension and fever were observed The number time antegraderetrograde prehabilitation operation adverse reactions during the operation and other special conditions were recorded every day and the weight of the patient was recordedPatients in the control group received routine perioperative management

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None