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RECRUITINGOBSERVATIONAL

Patient Reported Outcomes Following Cancer of the Rectum

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The surgical management of rectal cancer includes a Total Mesorectal Excison (TME); depending on the height of the tumor, the problem of preservation of the anal sphincter arises, being able to perform a low anterior resection, an ultra-low anterior resection (RAUB) or an intersphincteric dissection. In some cases invading the sphincters or the puborectalis muscle, an abdominoperineal resection needs to be performed, being the gold standard in this particular situation so far. TME can be performed by open, laparoscopic, robotic or transanal approaches, as long as the oncological principles for the resection are achieved. Unfortunately, up to 90% of these patients will present a change in bowel habit, ranging from an increased frequency of bowel movements to the degree of fecal incontinence or evacuation dysfunction. Of these patients, 25-50% will have a severe alteration in the quality of life. This wide spectrum of symptoms has been called "low anterior resection syndrome" (LARS). Other collateral damage is the change in sexual and urinary function, due to hypogastric plexus injury. There is a significant lack of multicenter prospective studies that provide evidence, and that reveal the functional results and quality of life of these techniques available to date for the management of rectal cancer. The study is set up as a prospective multicentre observational study. Inclusion criteria are: 1) patients over 18 years old, 2) diagnosed with rectal cancer located below the peritoneal reflection, defined by preoperative MRI, 3) undergoing Open, laparoscopic, robotic or Transanal Total Mesorectal Excision (taTME) approaches, 4) with/without derivative stoma and 5) with/without neoadjuvant treatment. Exclusion criteria are: 1) Upper rectal cancer, located above the peritoneal reflection, 2) previous radical prostatectomy, 3) previous pelvic radiotherapy, 4) rectal resection without primary anastomosis, 5) intraoperative findings of peritoneal carcinomatosis, 6) stage IV disease, 7) multivisceral or en-bloc resection, which includes uterus, prostate, vagina or bladder, 8) rectal resection due to a benign condition, 9) rectal resection due to a recurrence of rectal cancer (previous anterior resection or another primary neoplasm), 10) rectal resection following a 'watch \& wait' program, 11) emergency surgery, 12) previous derivative colostomy 13) inflammatory bowel disease.

Who May Be Eligible (Plain English)

Who May Qualify: - Patients over 18 years old - willing to sign a consent form - Diagnosed with rectal cancer located below the peritoneal reflection, defined by preoperative MRI - Open, laparoscopic, robotic or Transanal Total Mesorectal Excision (taTME) approaches - Patients with/without derivative stoma - Patients with/without neoadjuvant treatment Who Should NOT Join This Trial: - Upper rectal cancer, located above the peritoneal reflection - Previous radical prostatectomy - Previous pelvic radiotherapy - Rectal resection without primary anastomosis - Intraoperative findings of peritoneal carcinomatosis - Stage IV disease - Multivisceral or en-bloc resection, which includes uterus, prostate, vagina or bladder - Rectal resection due to a benign condition - Rectal resection due to a recurrence of rectal cancer (previous anterior resection or another primary neoplasm) - Rectal resection following a 'watch \& wait' program - Emergency surgery - Previous derivative colostomy - Inflammatory bowel disease Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Patients over 18 years old * Informed consent * Diagnosed with rectal cancer located below the peritoneal reflection, defined by preoperative MRI * Open, laparoscopic, robotic or Transanal Total Mesorectal Excision (taTME) approaches * Patients with/without derivative stoma * Patients with/without neoadjuvant treatment Exclusion Criteria: * Upper rectal cancer, located above the peritoneal reflection * Previous radical prostatectomy * Previous pelvic radiotherapy * Rectal resection without primary anastomosis * Intraoperative findings of peritoneal carcinomatosis * Stage IV disease * Multivisceral or en-bloc resection, which includes uterus, prostate, vagina or bladder * Rectal resection due to a benign condition * Rectal resection due to a recurrence of rectal cancer (previous anterior resection or another primary neoplasm) * Rectal resection following a 'watch \& wait' program * Emergency surgery * Previous derivative colostomy * Inflammatory bowel disease

Treatments Being Tested

PROCEDURE

Open Total Mesorectal Excision

Open approach for Total Mesorectal Excision

PROCEDURE

Laparoscopic Total Mesorectal Excision

Laparoscopic approach for Total Mesorectal Excision

PROCEDURE

Robotic Total Mesorectal Excision

Robotic approach for Total Mesorectal Excision

PROCEDURE

Transanal Total Mesorectal Excision

Transanal approach for Total Mesorectal Excision

Locations (2)

University Clinic of Navarre
Madrid, Spain
University Hospital Gregorio Marañón
Madrid, Spain