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Completed

NCT Number: NCT02739516

Dual FSH/HCG Trigger in Letrozole Stimulated Intrauterine Insemination Cycles in Women With Unexplained Infertility

The objective of this study was to evaluate the outcome of follicle stimulating hormone (FSH) co-administration with human chorionic gonadotrophins trigger for women with unexplained infertility (UEI) and assigned for letrozole (LTZ) stimulated intrauterine insemination (IUI) cycles .

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

About this study

This prospective randomized controlled study included 108 women with unexplained infertility recruited among those attending the Gynecology Outpatient Clinics of, Benha University Hospital, and private settings, Alkalubia, Egypt from Jun 2013 to Aug 2015. The study protocol was approved by the Local Ethics Committee and written informed consents were taken from both partners before starting of the study.

All women received the same regimen of ovarian stimulation using Letrozole (Femara; Novartis pharma AG, Basle, Switzerland) 2.5 mg tab twice daily for 5 days starting from cycle day 3. Transvaginal ultrasound scan (TVS) was performed daily from cycle day 9 and a total of 10,000 IU of hCG (Epifasi, EPICO) was administered to those in whom at least one ovarian follicle was ≥18 mm in size. On the day of hCG administration women were randomly categorized into two groups according to a computer generated random numerical table. Envelopes containing the allocation information were chosen sequentially by patient herself in presence of her husband. Group A received FSH (urofollitropin; Fostimon, IBSA, Bazel, Swiz; 75 IU amp) 150 IU injected once on day of hCG injection and group B received no FSH on day of hCG injection. Intrauterine insemination was performed 36 hours after HCG injection. Women in both groups received luteal phase support in the form of vaginal progesterone, (Prontogest 400 mg Vaginal Pessaries, IBSA) twice a day, starting from the day after IUI and continued till the eighth week, if the pregnancy test was positive.Two weeks later, quantitative ßhCG was estimated to diagnose chemical pregnancy. However, TVS was performed 4 weeks after positive pregnancy test to confirm clinical pregnancy by the presence of gestational sac with fetal echoes and pulsation and to exclude ectopic pregnancy. All women enrolled in the study underwent the study protocol for three consecutive cycles unless got pregnant.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Unexplained infertility for more than 2 years
  • Normal ovulation proved by midluteal serum progesterone level >5 ng/ml,
  • Patent fallopian tubes confirmed by hysterosalpingography or laparoscopy
  • Normal semen analysis according to the modified World Health Organization (WHO) criteria
  • Normal hormonal profile (FSH, LH, prolactin and TSH) in the early follicular phase.

Exclusion criteria

  • Other causes of infertility ( tubal factors, polycystic ovary syndrome (PCOS), endometriosis)
  • Ovarian cysts,
  • FSH >10 mIU/ml.
  • Previous intrauterine insemination (IUI )cycles,
  • Liver or kidney diseases,
  • Hypersensitivity to the used medications.

Treatment and study plan

Human Chorionic Gonadotropin

Drug

In letrozole stimulated cycle; Human chorionic gonadotropin ( hCG) 10000 IU was given intramuscular when the mean ovarian follicle diameter was ≥18 mm.

FSH co-trigger

Drug

In letrozole stimulated cycle; FSH (urofollitropin; Fostimon, IBSA, Bazel, Swiz; 75 IU amp) 150 IU injected once intramuscular when the mean ovarian follicle diameter was ≥18 mm.

letrozole

Drug

Letrozole oral tablets (Femara 2.5 mg tablet; Novartis Pharma Services, Switzerland) 2.5 mg tab twice daily for 5 days from cycle day 3.

Primary outcomes

  1. Clinical pregnancy rate per cycle (PR/C) and per woman (PP/W)

    Time frame: Throughout the study completion; up to 3 months

    Achievement of clinical pregnancy defined as the presence of an intrauterine gestational sac with a pulsating fetal heart beat on ultrasound

Secondary outcomes

  1. Frequency of ovarian hyperstimulation syndrome (OHSS)

    Time frame: Throughout the study completion; up to 3 months

    Number of participants developed ovarian hyperstimulation syndrome (OHSS) per all women received intervention

  2. Multiple pregnancies

    Time frame: Throughout the study completion; up to 3 months

    Number of participants had multiple pregnancy per women achieved pregnancy .

  3. The live birth rate per woman (LB/W).

    Time frame: Throughout the study completion; up to 2 year

    Number of live birth per women receiving intervention.

Sponsors and collaborators

Lead sponsor

Benha University

Other

Registry information

Official study title

Concomitant Administration of Follicle-stimulating Hormone at the Time of Human Chorionic Gonadotropin Trigger in Letrozole Stimulated Intrauterine Insemination Cycles in Women With Unexplained Infertility

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Apr 15, 2016
Registry last updated
May 19, 2016

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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