Improving Quality of Life of Prostate Cancer Survivors With Androgen Deficiency

Clinicaltrials.gov ID: NCT03716739
db-list-check Status RECRUITING
b-loader Phase PHASE2
b-people Age ≥ 40 Years
b-bullseye-arrow Enrollments 142

Conditions

Prostate Cancer

Drugs

Testosterone Cypionate 100 MG/ML, Placebo

Summary

The purpose of this phase II trial is to determine the efficacy and safety of testosterone replacement therapy (TRT) in improving the symptoms of androgen deficiency and health-related quality of life in men with prostate cancer who have undergone radical prostatectomy.

Detailed Description

The overall objective is to conduct a proof-of-concept double-blind, placebo-controlled, parallel group, randomized trial to determine the efficacy and safety of testosterone replacement therapy (TRT) in improving the symptoms of androgen deficiency (sexual symptoms, low energy, and physical dysfunction) and overall health-related quality of life in men with prostate cancer who have undergone radical prostatectomy for organ-localized disease (pT2,N0,M0), Gleason score < 7 (3+4), who have undetectable PSA (<0.1 ng/mL using a sensitive PSA assay) for > 2 years after radical prostatectomy, and who have androgen deficiency.

Locations

3 locations Found with status Recruiting

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Shalender Bhasin, MD

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Shalender Bhasin, MD

Status

  • RECRUITING

Contact Person

  • Shalender Bhasin

Principal Investigator

  • Shalender Bhasin, MD

Eligibility Criteria

Inclusion Criteria:

Men with prostate cancer, who have Stage pT2, N0, M0 lesions (confined to the gland); Combined Gleason score of 7 (3+4 elements) or less; Preoperative PSA less than 10 ng/ml; Stable and undetectable PSA level (PSA less than 0.1 ng/mL using an assay that has a functional sensitivity of 0.1 ng/mL) for at least two years after radical prostatectomy.

* Age: 40 years and older
* Presence of symptoms related to sexual dysfunction, fatigue/low vitality, or physical dysfunction.
* An average of two fasting, early morning serum testosterone levels, measured by LC-MS/MS, less than 275 mg/dL and/or free testosterone by equilibrium dialysis <60 pg/mL. middle-aged and older men with mean testosterone levels > 300 ng/dL.
* Ability and willingness to provide informed consent

Exclusion Criteria:

* Men who have undergone radiation therapy
* Men receiving androgen deprivation therapy will be excluded.
* Hemoglobin <10 g/dL or >16.5 g/dL
* Severe untreated sleep apnea
* Allergy to sesame oil
* Uncontrolled heart failure
* Myocardial infarction, acute coronary syndrome, revascularization surgery, or stroke within 3 months
* Serum creatinine >2.5 mg/dL; ALT 3x upper limit of normal;
* Hemoglobin A1c >7.5% or diabetes requiring insulin therapy
* Body mass index (BMI) >40 kg/m2
* Untreated depression. Subjects with depression who have been on stable anti-depressant medication, or undergoing CBT for more than three months are eligible.
* Men with axis I psychiatric disorder, such as schizophrenia, will be excluded.
* Subjects who have used the following medications within the past 6 months: testosterone, DHEA, estrogens, GnRH analogs, antiandrogens, spironolactone, ketoconazole, rhGH, megestrol acetate, prednisone 20 mg daily or equivalent doses of other glucocorticoids for more than two weeks

Study Plan

Treatment Arm

ACTIVE_COMPARATOR

Weekly IM administration of 100 mg testosterone cypionate for 12 weeks.

  • DRUG:

    Testosterone Cypionate 100 MG/ML

    Description:

    100 mg testosterone cypionate administered by intramuscular injection weekly for 12 weeks.

Control Arm

PLACEBO_COMPARATOR

Weekly IM administration of placebo for 12 weeks.

  • DRUG:

    Placebo

    Description:

    Placebo administered by intramuscular injection weekly for 12 weeks.

Outcome Measures

Primary Outcome Measures

Change in sexual activity

Time Frame: 5-8 months

Secondary Outcome Measures

Change in erectile function

Time Frame: 5-8 months

Change in sexual desire

Time Frame: 5-8 months

Change in energy level

Time Frame: 5-8 months

Change in mood

Time Frame: 5-8 months

Change in physical function

Time Frame: 5-8 months

Change in self-reported physical function

Time Frame: 5-8 months

Change in maximal voluntary strength

Time Frame: 5-8 months

Change in lean body mass

Time Frame: 5-8 months

Change in hormone Levels

Time Frame: 5-8 months

Change in aerobic capacity

Time Frame: 5-8 months

Timeline

  • Last Updated
    August 12, 2024
  • Start Date
    October 23, 2018
  • Today
    February 5, 2025
  • Completion Date ( Estimated )
    June 1, 2025

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