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Nerve Grafting With an Allograft During Radical Prostatectomy - Extended Follow-up in a Prospective Randomized Trial

Primary Purpose

Erectile Dysfunction Following Radical Prostatectomy

Status
Terminated
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Radical prostatectomy with implantation of allograft
Radical prostatectomy without implantation of allograft
Sponsored by
Kantonsspital Winterthur KSW
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Erectile Dysfunction Following Radical Prostatectomy focused on measuring radical prostatectomy, erectile function, nerve grafting, allogenic, prostate cancer, Allogenic nerve graft, Time required for nerve grafting

Eligibility Criteria

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

Inclusion Criteria:

  • Localized intermediate-risk or high-risk prostate cancer cT3
  • Gleason score ≥ 7 (3+4 and/or 4+3) and/or
  • PSA ≥ 20 ng/ml
  • intact preoperative erectile function with an IIEF ≥ 21 (IIEF-6).

Exclusion Criteria:

  • IIEF < 21
  • Operations in the past 6 months which could limit the erectile function
  • Erectile dysfunction in the history or current medication for erectile dysfunction
  • Current involvement in another comparable study.

Sites / Locations

  • Kantonsspital Winterthur

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Control group

Treatment group

Arm Description

Radical prostatectomy without implantation of allograft

Radical prostatectomy with implantation of allograft

Outcomes

Primary Outcome Measures

Erectile function score (IIEF: international index of erectile function) after non nerve sparing radical prostatectomy
Erectile function score (IIEF: international index of erectile function) after non nerve sparing radical prostatectomy. To show a complete impotence in the control group and an enhancement of the initial postoperative impotence in the treatment group

Secondary Outcome Measures

Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Monitoring of side effects and complications in connection with the nerve-implantation.

Full Information

First Posted
December 13, 2012
Last Updated
February 18, 2021
Sponsor
Kantonsspital Winterthur KSW
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1. Study Identification

Unique Protocol Identification Number
NCT01770340
Brief Title
Nerve Grafting With an Allograft During Radical Prostatectomy - Extended Follow-up in a Prospective Randomized Trial
Official Title
Nerve Grafting With an Allograft During Radical Prostatectomy - Extended Follow-up in a Prospective Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Terminated
Why Stopped
Poor recruitment, Interim analysis: The rates of pts who reached primary and secondary endpoints were lower than expected.
Study Start Date
January 2011 (undefined)
Primary Completion Date
April 2017 (Actual)
Study Completion Date
July 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kantonsspital Winterthur KSW

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Earlier studies were able to show that an improvement of the erectile function following a non-nerve sparing radical prostatectomy could be achieved using an autologous nerve graft. The investigators evaluate the use of the implantation of the allogenic nerve graft Avance® in patients undergoing non nerve-sparing radical prostatectomy.
Detailed Description
In this prospective randomised and single-blind, clinical phase-IV study, 60 patients are randomized into the treatment group and the control group. The follow-up is at least 24 months. The inclusion criteria were localized prostate cancers cT3 and/or Gleason score ≥ 7 (a or b) and/or prostate-specific antigen (PSA) ≥ 20 ng/ml and furthermore an erectile function with an IIEF ≥ 21 (IIEF-6). The operation carried out is a standardised, robot assisted laparoscopic radical prostatectomy with total excision of both neurovascular bundles. The Outcome measurement is done with the "quality of life questionnaire before and after prostate surgery" that includes the "International Index of Erectile Function" (IIEF) questionnaire. The limitations are a small cohort, a short observation period and the lack of statistical analysis due to a still low number of patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Erectile Dysfunction Following Radical Prostatectomy
Keywords
radical prostatectomy, erectile function, nerve grafting, allogenic, prostate cancer, Allogenic nerve graft, Time required for nerve grafting

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Sham Comparator
Arm Description
Radical prostatectomy without implantation of allograft
Arm Title
Treatment group
Arm Type
Experimental
Arm Description
Radical prostatectomy with implantation of allograft
Intervention Type
Biological
Intervention Name(s)
Radical prostatectomy with implantation of allograft
Intervention Description
Interposition of resected neurovascular bundles with allograft Avance®
Intervention Type
Procedure
Intervention Name(s)
Radical prostatectomy without implantation of allograft
Intervention Description
No interposition of resected neurvascular bundles
Primary Outcome Measure Information:
Title
Erectile function score (IIEF: international index of erectile function) after non nerve sparing radical prostatectomy
Description
Erectile function score (IIEF: international index of erectile function) after non nerve sparing radical prostatectomy. To show a complete impotence in the control group and an enhancement of the initial postoperative impotence in the treatment group
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Description
Monitoring of side effects and complications in connection with the nerve-implantation.
Time Frame
24 months
Other Pre-specified Outcome Measures:
Title
Documented will be the extra time required for the nerve implantation
Description
How much operation-time takes the nerve implantation? The time is stopped which is required for the implantation of the nerve. Start is when the prostate was removed and was deposited in the extraction bag. Stop when the anastomosis of the nerves is stitched and the anastomosis of the urethra begins.
Time Frame
at the time of operation

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Localized intermediate-risk or high-risk prostate cancer cT3 Gleason score ≥ 7 (3+4 and/or 4+3) and/or PSA ≥ 20 ng/ml intact preoperative erectile function with an IIEF ≥ 21 (IIEF-6). Exclusion Criteria: IIEF < 21 Operations in the past 6 months which could limit the erectile function Erectile dysfunction in the history or current medication for erectile dysfunction Current involvement in another comparable study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hubert John, Chefarzt
Organizational Affiliation
Kantonsspital Winterthur KSW
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital Winterthur
City
Winterthur
State/Province
Kanton Zürich
ZIP/Postal Code
8401
Country
Switzerland

12. IPD Sharing Statement

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Nerve Grafting With an Allograft During Radical Prostatectomy - Extended Follow-up in a Prospective Randomized Trial

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