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Clinical Trials/NCT00752869
NCT00752869
Completed
Phase 4

Dutasteride in Men Receiving Testosterone Therapy: Impact on Serum PSA, Testosterone, DHT Levels and Prostate Volume: "Implications for Prostate Safety"

The Miriam Hospital2 sites in 1 country24 target enrollmentSeptember 2008

Overview

Phase
Phase 4
Intervention
placebo
Conditions
Hypogonadism
Sponsor
The Miriam Hospital
Enrollment
24
Locations
2
Primary Endpoint
PSA reduction
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

This is a study using two FDA approved medications: Testosterone and the study medication, Dutasteride (Avodart 0.5mg/day). Half of the subjects will receive dutasteride and half will receive a placebo. The study medication will be taken for 12 months.

The subjects participating in the study are men who are already taking their own testosterone supplement because they have low testosterone levels which may cause them to experience sexual function difficulties, have fatigue or other symptoms. Testosterone can have an adverse effect of causing an enlarged prostate (Benign Prostatic Hypertrophy) (BPH).

Dutasteride (Avodart) is an approved medication used to decrease the prostate size, prevent urinary symptoms and reduce the risk of surgery.

The researchers would like to see if by taking dutasteride and testosterone at the same time they can prevent the adverse effects of testosterone and at the same time get the positive benefits of testosterone.

There will be 6 scheduled visits for the study and 2 diagnostic tests called a TRUS (TransRectal UltraSound), to evaluate prostate size. The six visits at will include consenting, blood work, two sexual function questionnaires, a physical examination, physical measurements, study medication teaching and dispensing of study medication.

Detailed Description

Termination criteria 1. Serum AST or ALT \> 3 times ULN 2. Total serum bilirubin \> 1.5 times ULN * no study termination of a patient with documented Gilberts disease for an isolated bilirubin elevation unless it exceeds 2.5x the upper limit of normal. 3. Hematocrit \> 55% 4. Subject experiences any unacceptable or intolerable adverse effect. 5. Subject is non-compliant with the study protocol. 6. Subject needs to take any medication that would interfere with study measurements 7. Subject develops prostate or breast cancer

Registry
clinicaltrials.gov
Start Date
September 2008
End Date
March 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Martin M. Miner, MD

Principal Investigator

The Miriam Hospital

Eligibility Criteria

Inclusion Criteria

  • Subjects currently on stable testosterone replacement therapy for 3 months' duration using either the approved transdermal products Androgel® or Testim®, or injections of testosterone enanthate or cypionate with a morning serum testosterone concentration within the normal range (300 - 1000 ng/dl). These will dispensed either by prescription or for injections by the PI or co-PI in the office.
  • Total Serum PSA \>1.5 - 10 ng/mL
  • If the total serum PSA is \>4ng/mL, the investigator, or a qualified urologist, will perform a 12-core prostate biopsy prior to entry unless such a biopsy has already been performed within the past 6 months.
  • If the PSA rises above 4 during any time of the study, the patient will be referred to urology for biopsy.
  • Patients with any suspicious rise in PSA of \>1.0 ng/ml/yr will have a repeat PSA performed within one month of the original value. If the rise in PSA remains \>1.0 ng/ml/yr, the patient will undergo a prostate biopsy.
  • b. If the individual has had a negative biopsy more than 6 months previously, with documentation of stable PSA since that time, ie, no sustained increase \>1.0ng/ml.
  • Subject is able to read and comprehend the informed consent document.
  • If the subject is on current replacement therapy for hypopituitarism or other multiple endocrine abnormalities, the subject must be on stable doses of thyroid hormone and/or adrenal replacement hormones for at least 14 days prior to enrollment.

Exclusion Criteria

  • Use of medications including those interactive with dutasteride from prior studies
  • Hematocrit greater than 51%
  • Prostate cancer in men found to have a prostate nodule on initial exam and subsequent positive biopsy
  • No prostate surgery within 2 months of entry
  • No prior use of finasteride, dutasteride within 6 months prior
  • A history of hepatic impairment or abnormal liver function tests (defined as ALT, AST, alkaline phosphatase or bilirubin \>1.5 times the upper limit of normal) with the exception that bilirubin elevations up to 2.0 times the upper limit of normal in the presence of normal liver enzymes will be permitted in patients with documented Gilbert's Disease. Subjects with Gilbert's disease not to be excluded.
  • No serum creatinine greater than 2.0 times upper limit of normal
  • No history of alcohol abuse with last 12 months
  • Has received any medication in a clinical trial within 2 months of enrollment
  • Use of anti-androgens, estrogens or coumadin

Arms & Interventions

B

This group will meet the same inclusion and exclusion criteria as the group receiving the study drug

Intervention: placebo

A

This arm will receive the active medication dutasteride

Intervention: dutasteride

Outcomes

Primary Outcomes

PSA reduction

Time Frame: with up to 12 months of treatment

Secondary Outcomes

  • Prostatic TRUS pre and post treatment(1 year treatment)
  • PV reduction with up to 12 months of treatment(1 year treatment)
  • DHT and T levels: serum(1 year treatment)
  • IIEF; MHSQ: Questionnaires examining the domains of erectile and orgasmic function in men in the two treatment arms(1 year treatment)

Study Sites (2)

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