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Intra-operative Neuromodulation of the Pelvic Plexus

Primary Purpose

Erectile Dysfunction, Prostate Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Nerve Stimulation
Sponsored by
Laikο General Hospital, Athens
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Erectile Dysfunction focused on measuring Erectile Dysfunction, Prostate Cancer, Neuromodulation

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Scheduled for open radical prostatectomy procedure under total anesthesia.
  • Age 40 to 75 years old.
  • Able to read and understand patient information materials and willing to sign a written informed consent.

Exclusion Criteria:

  • Have been diagnosed with severe vasculogenic erectile dysfunction.
  • Have a prior history of pelvic surgery, trauma or irradiation therapy.
  • Have a penile prosthesis.
  • Have been diagnosed with neurologic diseases that may negatively impact erectile functions.
  • Currently having an active implantable device (such as a pacemaker).
  • Posses any other characteristics that, per the investigator's judgment, may increase the risk or impair data collection for the procedure/study.
  • Inability to provide a fully informed consent.

Sites / Locations

  • Laikon General Hospital of AthensRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Nerve Stimulation

Arm Description

Acute placement of electrodes and electrostimulation of the pelvic plexus nerves during open radical prostatectomy.

Outcomes

Primary Outcome Measures

Penile circumference increase in millimeters.
Change in penile circumference [mm] in response to electrical stimulation of the pelvic plexus nerves measured by a penile plethysmograph.

Secondary Outcome Measures

Anatomic location of stimulation site
The anatomic location of the stimulation site on the pelvic floor (determined by the surgeon).
Stimulation threshold in volts
Amplitude in volts of the electrical stimulation pulses to induce penile response.

Full Information

First Posted
January 24, 2018
Last Updated
February 7, 2018
Sponsor
Laikο General Hospital, Athens
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1. Study Identification

Unique Protocol Identification Number
NCT03425240
Brief Title
Intra-operative Neuromodulation of the Pelvic Plexus
Official Title
Intra-operative Neuromodulation of the Pelvic Plexus
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
September 10, 2014 (Actual)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Laikο General Hospital, Athens

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the feasibility of electrical stimulation of nerves responsible for erectile function to evoke penile erection after surgery to remove the prostate (prostatectomy).
Detailed Description
Prostate cancer is the main cancer in men. However, the survival rate for clinically localized prostate cancer is prominent mainly due to radical prostatectomy (RP), the gold standard treatment for non-metastatic cancers. Unfortunately, despite providing optimal cancer control, RP often lead to neuropraxia and persistent erectile dysfunction in approximately 80% of men 1 year after prostatectomy. Various erectile rehabilitation strategies have not been able to prove a beneficial action yet. However, electrical stimulation has been demonstrated to favour neuroregeneration and the functional recovery of neuromuscular systems and has been shown to induce and maintain penile erection in animals and humans. Therefore, electrical stimulation of the pelvic plexus nerves during radical prostatectomy is being investigated for its potential development into a treatment aimed at improving recovery of erectile function after prostatectomy. The primary objective of this study is to explore the feasibility of using a neurostimulation device post radical prostatectomy as a method for neurogenic erectile dysfunction treatment. During standard open radical prostatectomy, the pelvic plexus nerves will be electrically stimulated intraoperatively and the modification of penile circumference will be recorded. The secondary objective is to assess proper placement of the stimulation electrodes and stimulation parameters needed to achieve maximal change in penile circumference.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Erectile Dysfunction, Prostate Cancer
Keywords
Erectile Dysfunction, Prostate Cancer, Neuromodulation

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nerve Stimulation
Arm Type
Experimental
Arm Description
Acute placement of electrodes and electrostimulation of the pelvic plexus nerves during open radical prostatectomy.
Intervention Type
Device
Intervention Name(s)
Nerve Stimulation
Intervention Description
Acute placement of electrodes on the pelvic plexus to apply electrostimulation during open radical prostatectomy.
Primary Outcome Measure Information:
Title
Penile circumference increase in millimeters.
Description
Change in penile circumference [mm] in response to electrical stimulation of the pelvic plexus nerves measured by a penile plethysmograph.
Time Frame
5 minutes
Secondary Outcome Measure Information:
Title
Anatomic location of stimulation site
Description
The anatomic location of the stimulation site on the pelvic floor (determined by the surgeon).
Time Frame
5 to 15 minutes
Title
Stimulation threshold in volts
Description
Amplitude in volts of the electrical stimulation pulses to induce penile response.
Time Frame
5 to 15 minutes

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Scheduled for open radical prostatectomy procedure under total anesthesia. Age 40 to 75 years old. Able to read and understand patient information materials and willing to sign a written informed consent. Exclusion Criteria: Have been diagnosed with severe vasculogenic erectile dysfunction. Have a prior history of pelvic surgery, trauma or irradiation therapy. Have a penile prosthesis. Have been diagnosed with neurologic diseases that may negatively impact erectile functions. Currently having an active implantable device (such as a pacemaker). Posses any other characteristics that, per the investigator's judgment, may increase the risk or impair data collection for the procedure/study. Inability to provide a fully informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Spyridon Skoufias, MD
Phone
spyskouf@hotmail.com
Email
spyskouf@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ioannis Adamakis, MD
Organizational Affiliation
Laikon General Hospital of Athens
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Constantinos A. Constantinides, MD
Organizational Affiliation
Laikon General Hospital of Athens
Official's Role
Study Chair
Facility Information:
Facility Name
Laikon General Hospital of Athens
City
Athens
ZIP/Postal Code
11527
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Spyridon Skoufias, MD
Phone
spyskouf@hotmail.com
Email
spyskouf@hotmail.com

12. IPD Sharing Statement

Learn more about this trial

Intra-operative Neuromodulation of the Pelvic Plexus

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