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Collagen Implant (Biological Mesh) Versus GM Flap for Reconstruction of Pelvic Floor After ELAPE in Rectal Cancer (NEAPE)

Primary Purpose

Rectal Cancer, Defect of Floor of Lesser Pelvis

Status
Active
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Reconstruction with an acellular porcine dermal collagen implant (biological mesh)
Reconstruction with a gluteus maximus myocutaneous flap
Sponsored by
Umeå University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer focused on measuring rectal neoplasms, reconstructive surgical procedure, bioprosthesis, surgical flaps, locomotion, lesser pelvis

Eligibility Criteria

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

Inclusion Criteria:

  • Adult (18 years or older) rectal cancer patients where wide resection of pelvic floor muscles together with rectum and anal canal have made reconstruction of pelvic floor necessary i.e. primary suture of pelvic floor in the midline is not possible. Resection of coccyx is optional.

Exclusion Criteria:

  • Age less than 18 years
  • Very large resections including partial resection of sacrum and patients considered for bilateral flap reconstruction
  • Large concomitant resection of vaginal wall where total (vaginal) wound closure is not an option
  • Expected survival less than one year at operation
  • Patient do not sign informed consent document

Sites / Locations

  • Oulu University Hospital
  • Sunderby County Hospital
  • Skåne Universtiy Hospital
  • Karolinska University Hospital, Solna
  • Umeå University Hospital, Department of Surgical and Perioperative Sciences
  • Uppsala University Hospital
  • Västmanlands Sjukhus Västerås
  • Östersund Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Porcine collagen implant (biological mesh)

Gluteus maximus flap

Arm Description

Reconstruction with an acellular porcine dermal collagen implant (biological mesh).

Reconstruction with a gluteus maximus myocutaneous flap.

Outcomes

Primary Outcome Measures

Performance in Timed-Stands Test
Timed-Stands test is a combined measure of physical performance depending on at least muscle strength, balance, tenderness of gluteal skin and muscles and co-ordination of motion.

Secondary Outcome Measures

Change in physical performance
Change in Timed-Stands Test performance
Primary wound healing assessed with the Southampton Wound Assessment Scale
The Southampton Wound Assessment Scale is a validated measure of wound healing after surgery.
Complications according to classification by Dindo-Clavien
The Dindo-Clavien classification of surgical complications is a validated instrument.
Proportion of persistent perineal sinus or fistula
Proportion of patients with the wound healing defect of all patients in the particular study arm
Ability to sit
Ability to sit is graded with a scale in three degrees.
Change of pain and discomfort in gluteal region measured with VAS
A standard visual analogue scale (VAS) from 0-100 mm is used.
Pain and discomfort in gluteal region, spot measures with VAS
A standard visual analogue scale (VAS) from 0-100 mm is used.
Change of quality of life measured with EQ-5D and EORTC forms C30 and CR29
EQ-5D and EORTC are validated quality of life instruments
Quality of life spot measures
Quality of life at specified time points
Length of hospital stay
Length of index hospital stay in days.
Costs of surgical treatment
Hospital expenses converted to US$
Quality-adjusted life years (QALYs gained)
Quality adjusted life year (QALY) is calculated using an quality of life utility index at repeated time points. The utility index is adjusted for the relevant background population.
Local recurrence
Local recurrence of rectal cancer detected by clinical or radiological investigation

Full Information

First Posted
May 3, 2011
Last Updated
May 2, 2023
Sponsor
Umeå University
Collaborators
The Swedish Society of Medicine, Västerbotten County Council, Sweden
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1. Study Identification

Unique Protocol Identification Number
NCT01347697
Brief Title
Collagen Implant (Biological Mesh) Versus GM Flap for Reconstruction of Pelvic Floor After ELAPE in Rectal Cancer
Acronym
NEAPE
Official Title
Nordic Extended Abdominoperineal Excision (NEAPE) Study, a RCT Comparing a Porcine Acellular Dermal Collagen Implant (Biological Mesh) With a Gluteus Maximus Flap for Reconstruction of Pelvic Floor After ELAPE in Rectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 5, 2011 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
September 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Umeå University
Collaborators
The Swedish Society of Medicine, Västerbotten County Council, Sweden

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The trial compares two different techniques for reconstruction of the lesser pelvic floor after an extended abdominoperineal excision for locally advanced rectal cancer. The alternative reconstruction techniques in the trial are: a technique using a gluteus maximus myocutaneous flap or a technique using an acellular porcine collagen implant (biological mesh) The primary endpoint will be physical performance six months from operation and our hypothesis is that the technique using an acellular porcine implant will cause less impaired physical performance compared to the technique using a myocutaneous flap. The study is interventional, randomized and by definition a comparative effectiveness research project.
Detailed Description
Extended abdominoperineal excision (EAPE) of the rectum is the potentially curative operation for rectal carcinomas too low for primary anastomosis, especially if the levator and sphincter musculature is infiltrated. This enlarged operation, when the levator musculature is excised en bloc with the rectum, creates a large defect. Primary closure is often not possible, and reconstruction with prosthetic material or a myocutaneous flap is necessary to avoid a perineal hernia. Implantation of a collagen sheet (biological mesh) has shown preliminary good results and on the other hand, the use of a gluteus myocutaneous flap is routine in many clinics. There is a lack of scientific evidence to prove which method is better for the reconstruction of the lesser pelvic floor. The current study aims to compare the two reconstruction techniques. Centres that treat locally advanced rectal cancers with the extended abdominoperineal excision of rectum (EAPE)[Holm et al 2007] can participate provided that: the operative technique is standardized according to the study protocol the centre/unit has resources for examinations of participants by a physiotherapist or a nurse the centre/unit has one investigator in charge of the study locally the centre/unit has an operative volume that enables at least 6 patients to be included/randomised during the anticipated three year study phase for inclusions Centres that do not operate the rectal cancers included in this study can participate by arranging the preoperative examination and physical tests as well as follow-up of patients that are referred to other centres for the operation. In these cases the operating centre cares for the randomisation, operation and start of postoperative rehabilitation while the study follow-up and final rehabilitation can be completed at the patients' primary referral hospital. The primary referral hospital needs a site investigator in charge of study patients just like centres that do the operations. Patients with primary or recurrent cancers of rectal origin can be included but individual patients can be included only once. Concomitant therapies are allowed and preoperative or postoperative radiation therapy and/or chemotherapy may be given or not according to local multidisciplinary team (MDT) decisions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer, Defect of Floor of Lesser Pelvis
Keywords
rectal neoplasms, reconstructive surgical procedure, bioprosthesis, surgical flaps, locomotion, lesser pelvis

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Porcine collagen implant (biological mesh)
Arm Type
Experimental
Arm Description
Reconstruction with an acellular porcine dermal collagen implant (biological mesh).
Arm Title
Gluteus maximus flap
Arm Type
Active Comparator
Arm Description
Reconstruction with a gluteus maximus myocutaneous flap.
Intervention Type
Procedure
Intervention Name(s)
Reconstruction with an acellular porcine dermal collagen implant (biological mesh)
Intervention Description
Reconstruction of floor of lesser pelvis with an acellular porcine dermal collagen implant (biological mesh) after extended excision of rectum including levator muscles in advanced low rectal cancer.
Intervention Type
Procedure
Intervention Name(s)
Reconstruction with a gluteus maximus myocutaneous flap
Intervention Description
Reconstruction of floor of lesser pelvis with an gluteus maximus myocutaneous flap after extended excision of rectum including levator muscles in advanced low rectal cancer.
Primary Outcome Measure Information:
Title
Performance in Timed-Stands Test
Description
Timed-Stands test is a combined measure of physical performance depending on at least muscle strength, balance, tenderness of gluteal skin and muscles and co-ordination of motion.
Time Frame
6 months after surgery
Secondary Outcome Measure Information:
Title
Change in physical performance
Description
Change in Timed-Stands Test performance
Time Frame
3, 6 and 12 months after surgery compared with preoperative results
Title
Primary wound healing assessed with the Southampton Wound Assessment Scale
Description
The Southampton Wound Assessment Scale is a validated measure of wound healing after surgery.
Time Frame
3 months from operation
Title
Complications according to classification by Dindo-Clavien
Description
The Dindo-Clavien classification of surgical complications is a validated instrument.
Time Frame
3, 6 and 12 months after surgery
Title
Proportion of persistent perineal sinus or fistula
Description
Proportion of patients with the wound healing defect of all patients in the particular study arm
Time Frame
3, 6 and 12 months after surgery
Title
Ability to sit
Description
Ability to sit is graded with a scale in three degrees.
Time Frame
3, 6 and 12 months after surgery
Title
Change of pain and discomfort in gluteal region measured with VAS
Description
A standard visual analogue scale (VAS) from 0-100 mm is used.
Time Frame
3, 6 and 12 months after surgery compared to preoperative
Title
Pain and discomfort in gluteal region, spot measures with VAS
Description
A standard visual analogue scale (VAS) from 0-100 mm is used.
Time Frame
3, 6 and 12 months after surgery
Title
Change of quality of life measured with EQ-5D and EORTC forms C30 and CR29
Description
EQ-5D and EORTC are validated quality of life instruments
Time Frame
3, 6 and 12 months after surgery compared to preoperative
Title
Quality of life spot measures
Description
Quality of life at specified time points
Time Frame
3, 6 and 12 months after surgery
Title
Length of hospital stay
Description
Length of index hospital stay in days.
Time Frame
Six months after surgery
Title
Costs of surgical treatment
Description
Hospital expenses converted to US$
Time Frame
12 months after surgery
Title
Quality-adjusted life years (QALYs gained)
Description
Quality adjusted life year (QALY) is calculated using an quality of life utility index at repeated time points. The utility index is adjusted for the relevant background population.
Time Frame
12 months after surgery
Title
Local recurrence
Description
Local recurrence of rectal cancer detected by clinical or radiological investigation
Time Frame
Five years after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult (18 years or older) rectal cancer patients where wide resection of pelvic floor muscles together with rectum and anal canal have made reconstruction of pelvic floor necessary i.e. primary suture of pelvic floor in the midline is not possible. Resection of coccyx is optional. Exclusion Criteria: Age less than 18 years Very large resections including partial resection of sacrum and patients considered for bilateral flap reconstruction Large concomitant resection of vaginal wall where total (vaginal) wound closure is not an option Expected survival less than one year at operation Patient do not sign informed consent document
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Markku M Haapamäki, MD, PhD
Organizational Affiliation
Umeå University, Department of Surgical and Perioperative Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jörgen Rutegård, MD, PhD
Organizational Affiliation
Umeå University
Official's Role
Study Director
Facility Information:
Facility Name
Oulu University Hospital
City
Oulu
Country
Finland
Facility Name
Sunderby County Hospital
City
Luleå
ZIP/Postal Code
971 80
Country
Sweden
Facility Name
Skåne Universtiy Hospital
City
Malmö
ZIP/Postal Code
20502
Country
Sweden
Facility Name
Karolinska University Hospital, Solna
City
Stockholm
ZIP/Postal Code
171 76
Country
Sweden
Facility Name
Umeå University Hospital, Department of Surgical and Perioperative Sciences
City
Umeå
ZIP/Postal Code
901 85
Country
Sweden
Facility Name
Uppsala University Hospital
City
Uppsala
ZIP/Postal Code
751 85
Country
Sweden
Facility Name
Västmanlands Sjukhus Västerås
City
Västerås
ZIP/Postal Code
72189
Country
Sweden
Facility Name
Östersund Hospital
City
Östersund
ZIP/Postal Code
831 83
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
17143848
Citation
Holm T, Ljung A, Haggmark T, Jurell G, Lagergren J. Extended abdominoperineal resection with gluteus maximus flap reconstruction of the pelvic floor for rectal cancer. Br J Surg. 2007 Feb;94(2):232-8. doi: 10.1002/bjs.5489.
Results Reference
background
PubMed Identifier
21160320
Citation
Haapamaki MM, Pihlgren V, Lundberg O, Sandzen B, Rutegard J. Physical performance and quality of life after extended abdominoperineal excision of rectum and reconstruction of the pelvic floor with gluteus maximus flap. Dis Colon Rectum. 2011 Jan;54(1):101-6. doi: 10.1007/DCR.0b013e3181fce26e.
Results Reference
background
PubMed Identifier
31147361
Citation
Rutegard M, Rutegard J, Haapamaki MM. Multicentre, randomised trial comparing acellular porcine collagen implant versus gluteus maximus myocutaneous flap for reconstruction of the pelvic floor after extended abdominoperineal excision of rectum: study protocol for the Nordic Extended Abdominoperineal Excision (NEAPE) study. BMJ Open. 2019 May 29;9(5):e027255. doi: 10.1136/bmjopen-2018-027255.
Results Reference
derived

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Collagen Implant (Biological Mesh) Versus GM Flap for Reconstruction of Pelvic Floor After ELAPE in Rectal Cancer

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