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Patient Reported Outcomes Following Cancer of the Rectum

Patient Reported Outcomes Following Cancer of the Rectum

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04936581
Acronym
PROCaRe
Enrollment
200
Registered
2021-06-23
Start date
2021-09-01
Completion date
2028-09-30
Last updated
2024-01-23

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

Conditions

Rectal Cancer, Sphincter Ani Incontinence

Keywords

rectal cancer, taTME, laparoscopic TME, robotic TME, open TME, low anterior resection syndrome

Brief summary

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.

Detailed description

Accepting an alpha risk of 0.05 and a beta risk of 0.2 in a two-sided test, 45 subjects are necessary in first group and 45 in the second to recognize as statistically significant a difference greater than or equal to 2 units. The common standard deviation is assumed to be 3. It has been anticipated a drop-out rate of 20% Primary outcomes are LARS and Vaizey score. Secondary outcomes included are QLQ C30 and CR29, sexual function questionnaire (female/male), urinary function questionnaire and postoperative complications (Clavien-Dindo classification) Data will be collected in an online secure and protected repository (Castor edc). The planned study period is 2 years (September 2021 - September 2023). It is essential to have a validated instrument that allows us to assess sphincter function and the different aspects of quality of life in operated patients, since increased survival in this pathology has led to greater importance in the evaluation functional outcome and quality of life; Furthermore, there are recent studies that speak of the direct relationship between these factors.

Interventions

PROCEDUREOpen Total Mesorectal Excision

Open approach for Total Mesorectal Excision

Laparoscopic approach for Total Mesorectal Excision

Robotic approach for Total Mesorectal Excision

Transanal approach for Total Mesorectal Excision

Sponsors

University of Navarrra Hospital (Clinica Universitaria)
CollaboratorOTHER
Hospital de Leon
CollaboratorOTHER_GOV
Hospital del Rio Hortega
CollaboratorOTHER
University Hospital Gregorio Marañón
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Low anterior resection syndrome (LARS) score2022LARS score from 0-42 where 0 means better outcomes
Vaizey score2022Incontinence score from 0-28 where 0 means better outcomes

Secondary

MeasureTime frameDescription
Male sexual function2022IIEF questionnaire
Female sexual function2022FSFI questionnaires
QLQ C302022Quality of Life questionnaire
Postoperative complications2022Dindo-Clavien classification
Urinary function2022IPSS questionnaire
QLQ CR292022Quality of life questionnaire, colorectal cancer related

Countries

Spain

Contacts

Primary ContactPatricia Tejedor
patricia.tejedor@hotmail.com+34 91 586 7007
Backup ContactPatricia Tejedor
+34 91 586 7007

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026