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Early Closure of Temporary Ileostomy (EASY)

Primary Purpose

Rectal Cancer

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Early reversal of temporary ileostomy
Standard reversal of temporary ileostomy
Sponsored by
Herlev Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer focused on measuring Rectal cancer, Temporary ileostomy, Ealy reversal, Morbidity, Mortality, Quality of life, Economic effect

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with a temporary ileostomy after low anterior resection because of rectal cancer
  • Patients, who are physically and mentally fit to undergo surgery within 8-13 days

Exclusion Criteria:

  • Patients whose stoma is not reversible
  • Patients with diabetes
  • Patients being treated with Steroids
  • Patients with communicative problems
  • Patients with expected compliance issues

Sites / Locations

  • Herlev Hospital, University of Copenhagen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Early reversal group

Control group

Arm Description

Early reversal of temporary ileostomy

Standard reversal of temporary ileostomy

Outcomes

Primary Outcome Measures

Postsurgical morbidity
Patients are scored according to the Clavien-Dindo Classification of Surgical Complications.
Postsurgical morbidity
Patients are scored according to the Clavien-Dindo Classification of Surgical Complications.
Postsurgical morbidity.
Patients are scored according to the Clavien-Dindo Classification of Surgical Complications.

Secondary Outcome Measures

Quality of life
Patients quality of life is assessed with three questionnaires that supplement each other: Short Form 36 (SF-36), Ostomy Adjustment Scale (OAS) and European Organization for the Treatment of Cancer CR30+CR29 (EORTC QLQ-CR30+CR29)
Quality of life
Patients quality of life is assessed with three questionnaires that supplement each other: Short Form 36 (SF-36), Ostomy Adjustment Scale (OAS) and European Organization for the Treatment of Cancer CR30+CR29 (EORTC QLQ-CR30+CR29)
Quality of life
Patients quality of life is assessed with three questionnaires that supplement each other: Short Form 36 (SF-36), Ostomy Adjustment Scale (OAS) and European Organization for the Treatment of Cancer CR30+CR29 (EORTC QLQ-CR30+CR29)
Socio-economic effect of early reversal of temporary ileostomy
The investigators register all admissions to hospital and out-patient clinics up to 12 months after the operation. Furthermore, the investigators apply patients´self-reported data on visits to general practitioner, primary care nurses and other health care workers in primary care.
Socio-economic effect of early reversal of temporary ileostomy
The investigators register all admissions to hospital and out-patient clinics up to 12 months after the operation. Furthermore, the investigators apply patients´self-reported data on visits to general practitioner, primary care nurses and other health care workers in primary care.

Full Information

First Posted
January 28, 2011
Last Updated
January 16, 2016
Sponsor
Herlev Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01287637
Brief Title
Early Closure of Temporary Ileostomy
Acronym
EASY
Official Title
Early Closure of Temporary Ileostomy- a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Herlev Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study is being conducted as a prospective randomized controlled multicenter study of patients with a temporary ileostomy due to rectal cancer. The study will be conducted in hospitals in Denmark and Sweden under the framework of the Scandinavian Surgical Outcomes Group (www.ssorg.net). The study investigates the effect of reversing a temporary ileostomy after 8-13 days instead of later reversal more than 12 weeks after surgery.
Detailed Description
After creation of the temporary ileostomy patients are included and are randomized to two groups. Patients in the intervention group will have the stoma closed 8-13 days after stoma creation and will be compared to patients in the control group where the stoma is closed after a minimum of 12 weeks (standard treatment in Denmark and Sweden). Before randomization the eligible patients undergo a CT of the rectum to visualise the anastomosis and possible leakage. Furthermore, the local investigators may choose to supplement the CT with a rectoscopy. The research group includes 89 patients over an expected period of 4 years. Both groups are examined for postoperative complications as well as stoma-related complications at discharge and 3, 6 and 12 months after stoma creation. The research group also examines the impact on patients´ health-related quality of life at 3, 6 and 12 months after stoma creation. Finally the socio-economic effect in both groups will be analyzed and compared 6 and 12 months after stoma creation. An interim analysis is planned for safety as well as recalculation of statistical power.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer
Keywords
Rectal cancer, Temporary ileostomy, Ealy reversal, Morbidity, Mortality, Quality of life, Economic effect

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
89 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Early reversal group
Arm Type
Experimental
Arm Description
Early reversal of temporary ileostomy
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Standard reversal of temporary ileostomy
Intervention Type
Procedure
Intervention Name(s)
Early reversal of temporary ileostomy
Other Intervention Name(s)
stoma reversal 8-13 days post surgery
Intervention Description
Temporary ileostomy is reversed 8-13 days after the primary surgery
Intervention Type
Procedure
Intervention Name(s)
Standard reversal of temporary ileostomy
Other Intervention Name(s)
stoma reversal 12-26 weeks after stoma creation
Intervention Description
Patients in the control group will have the ileostomy reversed according to standard treatment, which is 12-26 weeks after primary operation
Primary Outcome Measure Information:
Title
Postsurgical morbidity
Description
Patients are scored according to the Clavien-Dindo Classification of Surgical Complications.
Time Frame
3 months after inclusion
Title
Postsurgical morbidity
Description
Patients are scored according to the Clavien-Dindo Classification of Surgical Complications.
Time Frame
6 months after inclusion
Title
Postsurgical morbidity.
Description
Patients are scored according to the Clavien-Dindo Classification of Surgical Complications.
Time Frame
12 months after inclusion-
Secondary Outcome Measure Information:
Title
Quality of life
Description
Patients quality of life is assessed with three questionnaires that supplement each other: Short Form 36 (SF-36), Ostomy Adjustment Scale (OAS) and European Organization for the Treatment of Cancer CR30+CR29 (EORTC QLQ-CR30+CR29)
Time Frame
Quality of life is assessed at 3 months after inclusion
Title
Quality of life
Description
Patients quality of life is assessed with three questionnaires that supplement each other: Short Form 36 (SF-36), Ostomy Adjustment Scale (OAS) and European Organization for the Treatment of Cancer CR30+CR29 (EORTC QLQ-CR30+CR29)
Time Frame
Quality of life is assessed at 6 months after inclusion
Title
Quality of life
Description
Patients quality of life is assessed with three questionnaires that supplement each other: Short Form 36 (SF-36), Ostomy Adjustment Scale (OAS) and European Organization for the Treatment of Cancer CR30+CR29 (EORTC QLQ-CR30+CR29)
Time Frame
Quality of life is assessed at 12 months after inclusion
Title
Socio-economic effect of early reversal of temporary ileostomy
Description
The investigators register all admissions to hospital and out-patient clinics up to 12 months after the operation. Furthermore, the investigators apply patients´self-reported data on visits to general practitioner, primary care nurses and other health care workers in primary care.
Time Frame
The investigators assess and analyze the economic effect 6 months after inclusion
Title
Socio-economic effect of early reversal of temporary ileostomy
Description
The investigators register all admissions to hospital and out-patient clinics up to 12 months after the operation. Furthermore, the investigators apply patients´self-reported data on visits to general practitioner, primary care nurses and other health care workers in primary care.
Time Frame
The investigators assess and analyze the economic effect 12 months after inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a temporary ileostomy after low anterior resection because of rectal cancer Patients, who are physically and mentally fit to undergo surgery within 8-13 days Exclusion Criteria: Patients whose stoma is not reversible Patients with diabetes Patients being treated with Steroids Patients with communicative problems Patients with expected compliance issues
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jacob Rosenberg, Professor
Organizational Affiliation
Herlev Hospital, University of Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Herlev Hospital, University of Copenhagen
City
Herlev
ZIP/Postal Code
2730
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
30911920
Citation
Park J, Angenete E, Bock D, Correa-Marinez A, Danielsen AK, Gehrman J, Haglind E, Jansen JE, Skullman S, Wedin A, Rosenberg J. Cost analysis in a randomized trial of early closure of a temporary ileostomy after rectal resection for cancer (EASY trial). Surg Endosc. 2020 Jan;34(1):69-76. doi: 10.1007/s00464-019-06732-y. Epub 2019 Mar 25.
Results Reference
derived
PubMed Identifier
29168881
Citation
Park J, Danielsen AK, Angenete E, Bock D, Marinez AC, Haglind E, Jansen JE, Skullman S, Wedin A, Rosenberg J. Quality of life in a randomized trial of early closure of temporary ileostomy after rectal resection for cancer (EASY trial). Br J Surg. 2018 Feb;105(3):244-251. doi: 10.1002/bjs.10680. Epub 2017 Nov 23.
Results Reference
derived
PubMed Identifier
27322187
Citation
Danielsen AK, Park J, Jansen JE, Bock D, Skullman S, Wedin A, Marinez AC, Haglind E, Angenete E, Rosenberg J. Early Closure of a Temporary Ileostomy in Patients With Rectal Cancer: A Multicenter Randomized Controlled Trial. Ann Surg. 2017 Feb;265(2):284-290. doi: 10.1097/SLA.0000000000001829.
Results Reference
derived
PubMed Identifier
22021780
Citation
Danielsen AK, Correa-Marinez A, Angenete E, Skullmann S, Haglind E, Rosenberg J; SSORG (Scandinavian Outcomes Research Group). Early closure of temporary ileostomy--the EASY trial: protocol for a randomised controlled trial. BMJ Open. 2011 Jul 29;1(1):e000162. doi: 10.1136/bmjopen-2011-000162.
Results Reference
derived

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Early Closure of Temporary Ileostomy

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