Skip to main content
Clinical Trials/NCT01578473
NCT01578473CompletedPhase 1

An Open-Label, Nine-Month Randomized Controlled Study of Testosterone (Testopel) Pellets Plus Vitamin D and E Versus Vitamin D and E Alone for the Treatment of Peyronie's Disease

Men's Health Boston1 site in 1 country75 target enrollmentStarted: May 23, 2013Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
75
Locations
1
Primary Endpoint
penile curvature

Study Overview

Brief Summary

Two recent studies have identified low levels of serum testosterone in association with Peyronie's Disease (PD), with a significant correlation noted between severity of testosterone deficiency and severity of curvature. The study hypothesis is to determine whether treatment with testosterone may help men with PD and penile curvature.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • acquired penile curvature of > 30 degrees and < 90 degrees associated with palpable penile plaque on physical examination
  • onset of curvature within 18 months prior to signing consent form
  • serum TT < 500 ng/dl at the screening visit

Exclusion Criteria

  • prior history of treatment for PD that includes intra-lesional injections, topical creams, or surgery
  • prior treatment with oral therapy at least 2 weeks prior to signing consent form (e.g. Potaba, Vitamin E, colchicines) will be acceptable for inclusion
  • prior history of treatment for testosterone deficiency
  • presence of dense calcified plaque by US or plain radiograph
  • taking the medication Coumadin
  • hypersensitivity to testosterone, stearic acid, or polyvinyl pyrolidone (the constituents of Testopel)
  • unable to achieve adequate erection with penile injection to access degree of curvature
  • undergone definitive treatment for prostate cancer, bladder cancer, or other pelvic malignancies including surgery, external beam radiation therapy, brachytherapy, cryotherapy.
  • prior history of prostate cancer, hematologic disorders, chronic liver disease including cirrhosis and hepatitis C, disorders affecting the immune system, including infection with human immunodeficiency virus, or psychiatric disorders including major depression, schizophrenia, bipolar disease
  • history of cerebrovascular accident, history of deep venous thrombosis within the past 5 years or history of untreated or severe sleep apnea
  • PSA > 4.0 ng/dL at the screening visit, unless prostate cancer has been excluded to the investigator's satisfaction
  • clinically significant abnormal lab results that would put the subject at increased risk or compromise the integrity of the study data, in the opinion of the investigator
  • received any other investigational drug within 30 days

Arms & Interventions

Vitamin D and E

Active Comparator

Oral Vitamin D and E alone in men with penile curvature due to PD.

Intervention: Vitamin D2 (Drug)

Vitamin D and E

Active Comparator

Oral Vitamin D and E alone in men with penile curvature due to PD.

Intervention: Vitamin E (Drug)

Testosterone Pellets and Vitamin D and E

Active Comparator

Testosterone in combination with oral Vitamin D an E supplementation in men with penile curvature due to PD.

Intervention: Testosterone Pellets (Drug)

Outcomes

Primary Outcomes

penile curvature

Time Frame: 9 months

The primary outcome to be assessed will be the change in penile curvature from baseline.

Secondary Outcomes

  • sexual function(9 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Abraham Morgentaler

Associate Clinical Professor of Urology Harvard Medical School

Men's Health Boston

Study Sites (1)

Loading locations...

Similar Trials

Testosterone Pellets Plus Vitamin D and E... | Clinical Trial