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Pilot Study for Evaluation of the Need for Protective Ileostomy After Low Anterior Resection Due to Rectal Cancer

H

Heidelberg University

Status and phase

Terminated
Phase 2

Conditions

Rectal Cancer

Treatments

Procedure: protective ileostomy

Study type

Interventional

Funder types

Other

Identifiers

NCT00457327
433/2005

Details and patient eligibility

About

The purpose of this study is to determine whether protective ileostomy is required after low anterior resection due to rectal cancer

Full description

Since introduction of total mesorectal excision prognosis and quality of life of patients with rectal cancer of the middle or lower third of the rectum could be improved significantly. There is no valid data about the need of protective ileostomy in these patients. About 10% of the patients develop insufficiency of the anastomosis and might benefit from ileostomy whereas about 90% would not have required protective ileostomy retrospectively. Aim of the study is to show that protective ileostomy is not required if several criteria are fulfilled and early measures in case of clinical impairment are defined. Therefore eligibility criteria include safely performed stapler anastomosis with complete rings and control of impermeability by air insufflation. In the event of clinical impairment in the postoperative course CT scan with KM filling of the rectum to exclude insufficiency of the anastomosis will be performed. In case of insufficiency protective ileostomy will be created. 40 patients will be included.

Comparison: Patients with resectable rectal cancer of the middle or lower third will be intraoperatively randomized to either protective ileostomy or no ileostomy at all.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • radical resectable rectal cancer
  • low sphincter-preserving resection of carcinomas of the lower and middle third
  • preoperative normal continence
  • preoperative normal sphincter function
  • complete rings after stapler anastomosis
  • impermeability of anastomosis for air
  • written informed consent

Exclusion criteria

  • reduced cooperation or drug abuse
  • pregnancy
  • psychosis
  • age under 18 years

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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