Skip to main content
Clinical Trials/NCT01766661
NCT01766661
Unknown
Not Applicable

Prospective Multicenter Randomized Controlled Trial Comparing Postoperative Complications and Quality of Life in Low Rectal Cancer Surgery Between Coloanal Anastomosis and Lateral Ileostomy Versus Two-Stage Turnbull-Cutait Coloanal Anastomosis

Hospital Universitari de Bellvitge4 sites in 2 countries92 target enrollmentJanuary 2013
ConditionsRectal Neoplasm

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rectal Neoplasm
Sponsor
Hospital Universitari de Bellvitge
Enrollment
92
Locations
4
Primary Endpoint
post-operative morbidity
Last Updated
7 years ago

Overview

Brief Summary

The aim of this study is to decrease the morbidity by 30% using the Turnbull-Cutait procedure in comparison to the standard surgery for low rectal cancer. The investigators compare quality of life, faecal incontinence and recurrence of neoplasm in patients who received standard colo-anal anastomosis with protective ileostomy or two-staged Turnbull-Cutait colo-anal anastomosis after Low Anterior Resection for rectal cancer.

Detailed Description

Anastomotic leak represents the most frequent complication after rectal cancer surgery and a lateral covering ileostomy is usually performed to reduce its incidence. Other important consequences of rectal cancer surgery are alterations in bowel habits and function and a negative impact on quality of life. This prospective, randomized, multicenter and controlled trial compares post-operative complications, quality of life, faecal incontinence and recurrence rate in patients treated for low rectal cancer with colo-anal anastomosis protected by a lateral ileostomy or with a two-staged Turnbull-Cutait colo-anal anastomosis.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
February 2022
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital Universitari de Bellvitge
Responsible Party
Principal Investigator
Principal Investigator

Sebastiano Biondo

PhD, MD

Hospital Universitari de Bellvitge

Eligibility Criteria

Inclusion Criteria

  • Patients with adenocarcinoma of the lower-middle third of the rectum proctoscopy established by rigid proctoscopy, with histological confirmation and candidates of colo-anal anastomosis;
  • Patients over 18 years and under 75 years, who can tolerate neoadjuvant and surgical treatment;
  • Patients who undergo an ultra-low anterior rectal resection with total mesorectal excision and nerve and sphincter-sparing with curative intention
  • Any extension of the primary tumor (T 1-2-3-4) according to the TNM classification;
  • Patients with or without lymph node metastasis (N - / +) and with or without resectable distant metastases;
  • Patients clinically without fecal incontinence prior to the current illness and with a Wexner incontinence Score less than or equal to 5;
  • Patients ASA I, II or III and adequate hematological, renal and hepatic function;
  • Patients who signed informed consent.

Exclusion Criteria

  • Altered cognitive state(eg mental retardation or dementia) that prevents collaboration in the study or patients who can neither read nor write
  • Fecal incontinence (Wexner equal to or greater than 6);
  • Previous surgery or proctological, colonic and anorectal functional disease
  • Diagnosis of synchronous colorectal or any other active neoplasm;
  • Patients ASA IV, V;
  • Pregnancy and lactation;
  • Rejection of the patient to sign the consent form.

Outcomes

Primary Outcomes

post-operative morbidity

Time Frame: within the first 30 days after surgery

Secondary Outcomes

  • local and/or distant recurrence of neoplasm(3 years)
  • Quality of life(3 years)
  • Fecal incontinence(3 years)

Study Sites (4)

Loading locations...

Similar Trials