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Completed

NCT Number: NCT01832168

Randomized Clinical Trial Using Amniotic Membrane in Robotic Assisted Laparoscopic Prostatectomy

The purpose of this study is to determine whether the AmnioFix dehydrated human amniotic membrane is effective in protecting nerves in men receiving robotic assisted laparoscopic prostatectomies.

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Key information

Conditions

Age range

45 year–70 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Jackson South Urology Center of Excellence

Miami, Florida, 33176, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ages 45-70
  • Clinically localized prostate cancer with Gleason score 6 or 7
  • SHIM Score greater than or equal to 16 in the absence of medication
  • Feasibility to perform unilateral or bilateral nerve sparing RALP

Exclusion criteria

  • Clinically locally advanced cancer and/or with Gleason score 8 or 9.
  • Difficulty performing nerve sparing RALP.
  • Prior surgery at the site.
  • Site exhibits clinical signs and symptoms of infection.
  • SHIM score at screening <16.
  • Current use of anticoagulant medication including Coumadin, Plavix, etc.
  • Has had "salvage prostatectomy" - patients who failed prior therapies including external radiation therapy, cryotherapy, etc.
  • Has prior radiation therapy treatment at the site.
  • Prior hormonal therapy such as Lupron or oral anti-androgens.
  • Non-mobile, i.e. not ambulatory or bed ridden.
  • The presence of comorbidities that can be confused with or can exacerbate the condition including:
  • diabetes
  • advanced atherosclerotic vascular disease
  • Patients with a history of more than two weeks treatment with immuno-suppressants (including systemic corticosteroids), cytotoxic chemotherapy within one month prior to initial screening, or who receive such medications during the screening period, or who are anticipated to require such medications during the course of the study.
  • Patients on any investigational drug(s) or therapeutic device(s) within 30 days preceding screening.
  • Unable to comply with penile rehabilitation.
  • Known history of having Acquired Immunodeficiency Syndrome (AIDS) or HIV.
  • Patients who are unable to understand the aims and objectives of the trial.
  • Presence of any condition(s) which seriously compromises the subject's ability to complete this study, or has a known history of poor adherence with medical treatment.
  • Currently taking medications which could affect graft incorporation (supervising physician's discretion).
  • Allergic to gentamicin and/or streptomycin.
  • Damage to neurovascular bundles during surgery.

Treatment and study plan

Robotic Assisted Laparoscopic Prostatectomy

Procedure

Robotic Assisted Laparoscopic Prostatectomy with nerve-sparing technique

Application of Absorbable Hemostat

Other

Application of Surgicel® SNoW Absorbable Hemostat by Johnson and Johnson on the neurovascular bundle after removal of the cancerous prostate.

Other names: Surgicel® SNoW

Application of dehydrated human amniotic membrane

Other

Application of dehydrated human amniotic membrane (DHAM) on the neurovascular bundle after removal of the cancerous prostate.

Other names: AmnioFix

Primary outcomes

  1. The proportion of patients achieving return to baseline Sexual Health Inventory for Men (SHIM) score in the AmnioFix group versus the Control group.

    Time frame: 4 weeks

Secondary outcomes

  1. Time to return of erectile function.

    Time frame: Up to 6 months

  2. Pain scores.

    Time frame: 10 days, 4 weeks, 3 months, and 6 months

Sponsors and collaborators

Lead sponsor

MiMedx Group, Inc.

Industry

Registry information

Official study title

A Prospective Randomized Clinical Trial Using Amniotic Membrane in Robotic Assisted Laparoscopic Prostatectomy (RALP)- Effect on Nerve Protection.

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Apr 15, 2013
Registry last updated
Mar 17, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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