Single Injection of Ganirelix in Gonadotropin Intrauterine Insemination (IUI) Cycles

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Ghassan F. Haddad, Houston Fertility Institute
ClinicalTrials.gov Identifier:
NCT01286051
First received: January 25, 2011
Last updated: March 19, 2013
Last verified: March 2013

January 25, 2011
March 19, 2013
January 2011
September 2012   (final data collection date for primary outcome measure)
Pregnancy rates [ Time Frame: One cycle of controlled ovarian stimulation (one month) ] [ Designated as safety issue: No ]
Follicle stimulating hormone (FSH) and IUI
Same as current
Complete list of historical versions of study NCT01286051 on ClinicalTrials.gov Archive Site
Premature leuteinizing hormone (LH) surge and ovulation [ Time Frame: One cycle of controlled ovarian stimulation (one month) ] [ Designated as safety issue: No ]
pregnancy rate in one cycle of FSH and single injection of GnRH antagonist
Same as current
Not Provided
Not Provided
 
Single Injection of Ganirelix in Gonadotropin Intrauterine Insemination (IUI) Cycles
Efficacy of Single Dose Ganirelix in Gonadotropin Ovulation Induction Cycles

Ovulation induction (OI) using gonadotropins is one of the most widely prescribed treatments of infertility. One common problem encountered while attempting OI using gonadotropins is premature ovulation. The purpose of this study is to examine the effect of a single injection of a medication, called ganirelix, to prevent premature ovulation. Patients will be divided into two groups. In the first group, gonadotropins will be used to stimulate the ovaries. In the second group gonadotropins will be used in addition to a single injection of ganirelix, a gonadotropin releasing hormone (GnRH) antagonist. Pregnancy rates will be compared between groups.

A randomized prospective study will be performed on patients attempting pregnancy using ovulation induction/intra-uterine insemination (IUI). Patients will be randomly assigned to one of two protocols:

Protocol A (control group): On menstrual cycle day 3, the patient will start gonadotropins (Follistim) injections at a starting dose of 75-150 IU and monitored according to the discretion of the treating physician. When the leading follicle reaches a size of at least 18mm, intramuscular human chorionic gonadotripin (hCG) (10,000 IU) is administered, followed by two inseminations, one at 12 hours after hCG, and the other at 36 hours. All patients will have luteal support using progesterone vaginal suppositories at a dose of 200mg two times per day (BID). Pregnancy testing will be scheduled at 2 weeks after the IUI. The treatment cycle typically lasts from 8-13 days, depending on the patient's response.

Protocol B (study group): On menstrual cycle day 3, the patient will start gonadotropins (Follistim) injections at a starting dose of 75-150 IU and monitored according to the discretion of the treating physician. When the leading follicle reaches a size of 13-14mm in mean diameter, or when the estradiol level reaches a level of 400 pg/ml, ganirelix injection at the standard dose of 250mcg is given once subcutaneously. When the leading follicle reaches a size of at least 18mm, intramuscular hCG (10,000IU) is administered followed by two inseminations, one at 12 hours after hCG, and the other at 36 hours. All patients will have luteal support using progesterone suppositories at a dose of 200mg BID. Pregnancy testing will be scheduled at 2 weeks after the IUI. The treatment cycle typically lasts from 8-13 days, depending on the patient's response.

Patients will be randomized, via computer generated program, in a 1:1 fashion.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Compare Pregnancy Rates Between FSH Stimulation and FSH and
  • GnRH Antagonist
  • Drug: Follistim administration
    adminstation of FSH for ovulation induction
    Other Name: Follistim
  • Drug: Follistim plus Ganirelix
    Follistim plus single injection of ganirelix
    Other Names:
    • Follistim
    • ganirelix
  • Active Comparator: Follistim
    standard treatment
    Intervention: Drug: Follistim administration
  • Experimental: Follistim plus single ganirelix injection
    Intervention: Drug: Follistim plus Ganirelix
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
80
September 2012
September 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients undergoing ovulation induction (OI) between ages 18 - 39 years.
  • One or more of the following infertility diagnoses: ovulation dysfunction, mild male factor infertility (sperm concentration of 5- 20 million/ml, and/or sperm motility 10% - 40%) , absence teratospermia (i.e. strict morphology > 4%), unexplained infertility.
  • Patent Fallopian tubes.
  • Normal uterine structure (i.e. absence of mullerian anomalies)
  • Ability to consent to the study.
  • Patients should be Houston Fertility Institute patients

Exclusion Criteria:

Exclusion criteria include:

  • Age 39 or above
  • Severe male factor (concentration < 10 million/ml or strict morphology < 4%)
  • Obstructed Fallopian tubes on one or both sides
  • Stage III or IV endometriosis
  • Elevated FSH level (>10 IU/L)
  • Low antral follicular count (< 4 antral follicles per ovary)
  • Any other contraindication for ovulation induction
  • Inability to consent to the study
  • History of any prior failed OI/IUI cycle
Female
18 Years to 39 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01286051
P08115
No
Ghassan F. Haddad, Houston Fertility Institute
Houston Fertility Institute
Not Provided
Principal Investigator: Ghassan F Haddad, M.D. Houston Fertility Institute
Houston Fertility Institute
March 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP