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Completed

NCT Number: NCT00891228

Study of the Safety, and Sperm and Gonadotropin Suppression of a Contraceptive Gel in Normal Men

To determine the number of men who have suppression of sperm production when using a daily regimen of Nestorone® Gel (0, 8 or 12 mg) and Testosterone Gel applied transdermally.

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Key information

Conditions

Age range

18 year–50 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Los Angeles Biomedical Research Institute at Harbor-UCLA, Torrance, California, United States

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Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Men who meet all the following criteria are eligible for enrollment in the trial:

  • Male volunteers in good health as confirmed by physical examination, medical history, and clinical laboratory tests of blood and urine at the time of screening
  • 18 to 50 years of age
  • BMI ≤ 33 calculated as weight in Kg/ (height in cm) 2
  • No history of hormonal therapy use in the last six months prior to the first screening visit
  • Subject will agree to use a recognized effective method of contraception with his partner (i.e. at a minimum, use double-barrier contraception) during the course of the study treatment and recovery phase
  • In the opinion of the investigator, subject is able to comply with the protocol, understand and sign an informed consent and HIPAA form
  • Does not meet any of the exclusion criteria.

Exclusion criteria

Men who meet any of the following criteria are NOT eligible for enrollment in the trial:

  • Men participating in another clinical trial involving an investigational drug within the last 30 days prior to the first screening visit
  • Men not living in the catchment's area of the clinic or within a reasonable distance from the site
  • Clinically significant abnormal findings at screening
  • Elevated PSA (levels ≥ 4 ng/mL), according to local laboratory normal values
  • Abnormal serum chemistry values, according to local laboratory normal values that indicate liver or kidney dysfunction or that may be considered clinically significant. Other abnormal lab values may also be exclusionary, at the discretion of the investigator
  • Sperm concentration below 15 million/mL in more than one of three screening samples
  • Use of androgens or body building substances within 6 months before first screening visit
  • Diastolic (D) blood pressure (BP) ≥ 85 and Systolic (S) BP ≥ 135 mm Hg; (BP will be taken 3 times at 5 minute intervals and the mean of all measurements be considered)
  • History of hypertension, including hypertension controlled with treatment
  • Known history of primary testicular disease or disorders of the hypothalamic-pituitary axis
  • Known hypersensitivity to progestins
  • Family or personal history of venous thromboembolism
  • Benign or malignant liver tumors; active liver disease
  • History of breast carcinoma
  • Known history of reproductive dysfunction including vasectomy or infertility
  • Known history of cardiac, renal, hepatic or prostatic disease
  • A serious systemic disease such as diabetes mellitus or morbid obesity (body weight greater than 120% of ideal body weight or BMI limitation as above)
  • History of sleep apnea
  • Known or suspected alcoholism or drug abuse that may affect metabolism/transformation of steroid hormones and study treatment compliance
  • Known dermatitis or severe skin disorder
  • Partner is known to be pregnant
  • Men desiring fertility within the first 24 weeks of study participation.

Men participating in competitive sports where drug screening for prohibited substances (including anabolic steroids) is routine will be advised of the relative and temporary hazards that participating in this study may have for their fertility or sporting status.

Treatment and study plan

Testosterone

Drug

Two individual packets of T Gel, each with 5 g of gel applied to each arm delivering a total of 100 mg of T on the skin daily.

Nestorone®

Drug

Nestorone® Gel will be delivered by a pump configured to deliver a metered volume of Nestorone® Gel containing 8 mg of Nestorone®. For 8 mg Nestorone® dose; Nestorone® Gel will be delivered in 4 mL volume (2 mg Nestorone® mL gel) by pressing two times with 2 mL dispenser head.

Primary outcomes

  1. The Number of Men Who Have Suppression of Sperm Production ≤1Million/mL Million/mL When Using a Daily Regimen of Nestorone® Gel (0, 8 or 12 mg) and Testosterone Gel Applied Transdermally.

    Time frame: 24 Weeks

Secondary outcomes

  1. The Number of Men Who Have Suppression of Sperm Production ≤3 Million/mL ≤ 3 Million/mL or Azoospermia When Using a Daily Regimen of Nestorone® Gel (0, 8 or 12 mg) and Testosterone Gel.

    Time frame: 24 Weeks

  2. The Number of Men Who Have Azoospermia

    Time frame: 24 Weeks

  3. The Impact on Sperm Motility in Men Who Are Not Azoospermic Azoospermic.

    Time frame: 24 Weeks

  4. The Impact on Sperm Morphology in Men Who Are Not Azoospermic

    Time frame: 24 weeks

Sponsors and collaborators

Lead sponsor

Premier Research

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • Population Council

Registry information

Official study title

A Multicenter, Randomized, Double-Blind Comparator Trial of the Safety and Sperm and Gonadotropin Suppression Resulting From Combined Use of Nestorone® Gel (0, 8 or 12 mg NES) and Testosterone Gel (10 g) Compared With Testosterone Gel in Normal Men

Acronym: CCN007

Important dates

Study start
2009
Primary completion
2010
Study completion
2011
First posted
May 1, 2009
Registry last updated
May 24, 2018

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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