Timing Evaluation of Stoma Closure (TIMES). Early vs Late Closure of Stoma After Rectal Cancer Surgery. (TIMES)
Primary Purpose
Rectal Cancer, Total Mesorectal Excision, Ileostomy - Stoma
Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Stoma closure
Sponsored by
About this trial
This is an interventional treatment trial for Rectal Cancer
Eligibility Criteria
Inclusion Criteria:
- Patients with rectal cancer (with / without metastasis) (with / without chemoterapy or radiotherapy)
- Patients undergoing low or ultra low anterior resection with anastomosis and stoma of protection.
- Patients with no intraoperative or postoperative complications.
- Radiological confirmation of the absence of anastomotic compilations (opaque enema or abdominal-pelvic CT scan with rectal contrast)
- Confirmation by rectoscopy of the absence of anastomotic compilations
Exclusion Criteria:
- Rectal cancer surgeries without anastomosis.
- Rectal cancer surgeries without stoma of protection.
Sites / Locations
- Hospital General Universitario de AlicanteRecruiting
- Complejo Hospitalario Universitario de CoruñaRecruiting
- Hospital General de ElcheRecruiting
- Hospital Josep TruetaRecruiting
- Hospital Gregorio MarañónRecruiting
- Hospital Ramón y CajalRecruiting
- Complejo Hospitalario de PontevedraRecruiting
- Hospital Univesitario de SalamancaRecruiting
- Hospital Universitari La FeRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Early stoma closure
Late stoma closure
Arm Description
Stoma closure 2-3 weeks after rectal surgery.
Stoma closure 16-24 weeks after rectal surgery.
Outcomes
Primary Outcome Measures
Determine and compare morbidity and mortality rates in patients with early and late stoma closure
Secondary Outcome Measures
Determine and analyze quality of life assisted by the SF36 scale in early vs late ileostomy closure
The SF36 is a short questionnaire with 36 items which measure eight multi-item variables: physical functioning (10 items), social functioning (two items), role limitations due to physical problems (four items), role limitations due to emotional problems (three items), mental health (five items), energy and vitality (four items), pain (two items), and general perception of health (five items). There is a further unscaled single item on changes in respondents' health over the past year. For each variable item scores are coded, summed, and transformed on to a scale from 0 (worst possible health state measured by the questionnaire) to 100 (best possible health state).
Full Information
NCT ID
NCT05284864
First Posted
August 6, 2020
Last Updated
March 8, 2022
Sponsor
Hospital Universitario La Fe
1. Study Identification
Unique Protocol Identification Number
NCT05284864
Brief Title
Timing Evaluation of Stoma Closure (TIMES). Early vs Late Closure of Stoma After Rectal Cancer Surgery.
Acronym
TIMES
Official Title
Timing Evaluation of Stoma Closure (TIMES). Early vs Late Closure of Stoma After Rectal Cancer Surgery.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitario La Fe
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to asses the safety and efficacy of early stoma closure (2-3 weeks after total mesorectal excision) vs late closure (16-24 weeks after mesorectal excision).
Detailed Description
Total mesorectal excision (TME) is considered the gold standard in obtaining a negative circumferential resection margin for cancers of the middle and lower third of the rectum. Despite all the oncological benefits,TME in ultra-low anterior resection carries some important drawbacks, such as a longer operative time, and its association with a higher rate of anastomotic leakage which increases in the most distal anastomoses.
Among the measures adopted to reduce mortality, the creation of protective ostomies has proven to be effective, however the protective ileostomy and its closure are not free of complications, such as dehydration and chronic kidney failure. In the investigator's country, various studies have analyzed this time to closure, being 10.8 months on average and with an increase in morbidity when closure is delayed the longest.
There are few prospective studies on the timing of stoma closure, which mainly focused on morbidity and mortality related to early closure. These studies did not demonstrate any significant negative effects on morbidity or mortality. The reason for early closure of the stoma is to reduce complications related to it. Although its true incidence is unknown, most patients have some type of stoma-related complication, which can be avoided or decreased in the case of early closure. In addition to the complications on the patient and their quality of life, the hospital costs secondary to them are not negligible.
The TIMES study ("TIMing Evaluation of Stoma closure") arises from the need to know the ideal moment for the closure of derivative stomata after rectal surgery.
Therefore, the hypothesis is that patients who undergo early ileostomy closure (at 2-3 weeks) after ultra-low anterior resection have fewer complications than patients with late ileostomy closure (4-6 months).
The main objective of this study is to analyze the morbidity and mortality associated with both early (early group, CASES group) and late closure (late group, CONTROL group) of the derivative ileosomy.
In this study, patients scheduled for temporary stoma closure after scheduled colorectal surgery will be randomized into two groups: early closure (14-21 days after surgery) or late closure (4th-6th month after surgery).
Patients will be followed from the time of study entry until 12 months after stoma closure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer, Total Mesorectal Excision, Ileostomy - Stoma, Ileostomy; Complications, Ileostomy Closure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Early stoma closure
Arm Type
Experimental
Arm Description
Stoma closure 2-3 weeks after rectal surgery.
Arm Title
Late stoma closure
Arm Type
Active Comparator
Arm Description
Stoma closure 16-24 weeks after rectal surgery.
Intervention Type
Procedure
Intervention Name(s)
Stoma closure
Intervention Description
Stoma closure after rectal surgery
Primary Outcome Measure Information:
Title
Determine and compare morbidity and mortality rates in patients with early and late stoma closure
Time Frame
From rectal surgery to stoma closure surgery
Secondary Outcome Measure Information:
Title
Determine and analyze quality of life assisted by the SF36 scale in early vs late ileostomy closure
Description
The SF36 is a short questionnaire with 36 items which measure eight multi-item variables: physical functioning (10 items), social functioning (two items), role limitations due to physical problems (four items), role limitations due to emotional problems (three items), mental health (five items), energy and vitality (four items), pain (two items), and general perception of health (five items). There is a further unscaled single item on changes in respondents' health over the past year. For each variable item scores are coded, summed, and transformed on to a scale from 0 (worst possible health state measured by the questionnaire) to 100 (best possible health state).
Time Frame
1 month, 6 month and 1 year after stoma closure surgery
Other Pre-specified Outcome Measures:
Title
Determine the patient's percentage with anterior resection syndrome, after early and late ileostomy closure assisted by the LARS scale.
Description
The LARS score has been validated and translated into several languages. By applying binomial regression on patient responses, the five issues that most bothered the patients were selected: incontinence for flatus, incontinence for liquid stool, frequency, clustering and urgency. Rating scale ranges from 0 to 42 points, and patients are classified into three groups: "no LARS" (0-20 points), "minor LARS" (21-29 points) and "major LARS" (30-42 points). According to the authors, the LARS score facilitates a fast identification of patients categorized as major LARS who will require treatment
Time Frame
1 month, 6 month and 1 year after stoma closure surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with rectal cancer (with / without metastasis) (with / without chemoterapy or radiotherapy)
Patients undergoing low or ultra low anterior resection with anastomosis and stoma of protection.
Patients with no intraoperative or postoperative complications.
Radiological confirmation of the absence of anastomotic compilations (opaque enema or abdominal-pelvic CT scan with rectal contrast)
Confirmation by rectoscopy of the absence of anastomotic compilations
Exclusion Criteria:
Rectal cancer surgeries without anastomosis.
Rectal cancer surgeries without stoma of protection.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David Abelló
Phone
+34630306333
Ext
412370
Email
davidabello1@gmail.com
Facility Information:
Facility Name
Hospital General Universitario de Alicante
City
Alicante
Country
Spain
Individual Site Status
Recruiting
Facility Name
Complejo Hospitalario Universitario de Coruña
City
Coruña
Country
Spain
Individual Site Status
Recruiting
Facility Name
Hospital General de Elche
City
Elche
Country
Spain
Individual Site Status
Recruiting
Facility Name
Hospital Josep Trueta
City
Girona
Country
Spain
Individual Site Status
Recruiting
Facility Name
Hospital Gregorio Marañón
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Name
Hospital Ramón y Cajal
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Name
Complejo Hospitalario de Pontevedra
City
Pontevedra
Country
Spain
Individual Site Status
Recruiting
Facility Name
Hospital Univesitario de Salamanca
City
Salamanca
Country
Spain
Individual Site Status
Recruiting
Facility Name
Hospital Universitari La Fe
City
Valencia
Country
Spain
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Timing Evaluation of Stoma Closure (TIMES). Early vs Late Closure of Stoma After Rectal Cancer Surgery.
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