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
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• aged 18-85 years old

• Karnofsky performance status (KPS)≥70%; Or ECOG score 2 points or less

• rectal cancer confirmed by preoperative pathology

• in the rectum resection before low, low colorectal anastomosis or after neoadjuvant therapy of patients

• prophylactic ileostomy.

Locations
Other Locations
China
the Affiliated Hospital of Qingdao
RECRUITING
Qingdao
Contact Information
Primary
Yanbing Zhou
zhouyanbing@qduhospital.cn
+86 137 0897 1773
Time Frame
Start Date: 2021-07-01
Estimated Completion Date: 2024-12
Participants
Target number of participants: 154
Treatments
Experimental: Prehabilitation Group
The contents of the ileostomy were collected and 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, antegrade/retrograde prehabilitation operation, adverse reactions during the operation and other special conditions were recorded every day, and the weight of the patient was recorded.
No_intervention: Perioperative management group
Perioperative management group
Related Therapeutic Areas
Sponsors
Leads: The Affiliated Hospital of Qingdao University

This content was sourced from clinicaltrials.gov