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Efficacy of stimulation of the efferent limb and rehabilitation procedure before ileostomy closure in rectal cancer patients underwent low anterior resection of rectum and temporary ileostomy: a randomized controlled single center study

Efficacy of stimulation of the efferent limb and rehabilitation procedure before ileostomy closure in rectal cancer patients underwent low anterior resection of rectum and temporary ileostomy: a randomized controlled single center study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050680
Enrollment
Unknown
Registered
2021-09-02
Start date
2021-09-10
Completion date
Unknown
Last updated
2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

???

Interventions

Experimental group:A set of preoperative preparation procedure (endoluminal draining after surgery + digital anal dilatation + efferent loop stimulation + anal sphincter exercise)
Control goup:Routine Waiting

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. Physical condition ECOG score 0-1; 3. Pathologically diagnosed rectal adenocarcinoma; 4. The distance between the lower edge of the tumor and the anal verge is less than or equal to 12cm (endoscopy) or the distance from the anorectal ring (ARJ) is less than or equal to 8cm; 5. Received neoadjuvant chemoradiotherapy before LAR; 6. Before participating in this study, sign the informed consent for the study; 7. Preoperative endoscopy to confirm that there is no anastomotic leakage before the closure of the ileostomy; 8. A protective ileostomy was added to the low anterior resection of rectal cancer and the return was completed 6 months after the operation.

Exclusion criteria

Exclusion criteria: 1. Patients with recurrent rectal cancer; 2. Liver cirrhosis or abnormal coagulation mechanism; 3. The individual lacks the ability of independent thinking, judgment and action, and cannot fill in the questionnaire as required; 4. The patient is a woman who is pregnant or breastfeeding; 5. The patient has other diseases or abnormal mental state, which may affect the patient's participation in this study.

Design outcomes

Primary

MeasureTime frame
sum of anastomotic stricture rate before ileostomy closure and rate of postoperative ileus after ileostomy.;

Secondary

MeasureTime frame
anastomotic leakage rate after ileostomy;time to resume diet after ileostomy ;time of hospital stay;low anterior resection syndrome score;recovery time of exsufflation and defecation;

Countries

China

Contacts

Public ContactZhan Tiancheng

Beijing Cancer Hospital

zlzhantiancheng@163.com+86 13911377261

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026