An Open Labeled RCT on the Effect of Additional hCG Injection for LPS on Pregnancy Outcomes in IHH Patients

Not Applicable

Recruiting

• Conditions: Luteal Phase Support; Idiopathic Hypogonadotropic Hypogonadism; Luteal Phase Deficiency
• Interventions: Drug: Additional hCG injection; Drug: estrogen and dydrogesterone

• Registration Number: NCT05569577
• Lead Sponsor: Fudan University

Brief Summary

Luteal phase deficiency (LPD) accounts for most failures of assistant artificial reproduction (ART) and early pregnancy loss for patients with idiopathic hypogonadotropic hypogonadism (IHH). Luteal phase support (LPS) is one of the indispensable interventions in ART treatments for IHH patients, which includes progestin, estrogen, human chorionic gonadotropin (hCG), and GnRH agonists (GnRHa). We aim to verify additional hCG injection 48 hours following routine hCG trigger and ovulation for LPS on the basis of supplementation of estrogen and dydrogesterone could improve clinical pregnancy rate, cumulative pregnancy rate, live birth rate and the prevalence of early pregnancy loss and ovarian hyperstimulation syndrome (OHSS) by an open labeled, prospective, and randomized clinical trial (RCT) in IHH patients in a single center.

Detailed Description

Idiopathic hypogonadotropic hypogonadism (IHH) is a congenital disease caused by a variety of gene variants leading to dysfunction in the secretion of hypothalamic gonadotropin-releasing hormones (GnRHs), with a prevalence of 1:125 000 in females. Girls with IHH often suffer from lack of puberty onset, amenorrhea and infertility, complicated with psychological problems such as depression and anxiety, due to delayed diagnosis and inappropriate treatment. Luteal phase deficiency (LPD) accounts for most failures of assistant artificial reproduction (ART) and early pregnancy loss for IHH patients. We have reported a severe LPD during the early trimester in a case with secondary HH following craniopharyngioma resection and speculated similar LPD happen in IHH patients complicated with low clinical pregnancy rate and live birth rate. Therefore, luteal phase support (LPS) is one of the indispensable interventions in ART treatments for IHH patients, which includes progestin, estrogen, human chorionic gonadotropin (hCG), and GnRH agonists (GnRHa). We aim to verify additional hCG injection 48 hours following routine hCG trigger and ovulation for LPS on the basis of supplementation of estrogen and dydrogesterone could improve clinical pregnancy rate, cumulative pregnancy rate, live birth rate and the prevalence of early pregnancy loss and ovarian hyperstimulation syndrome (OHSS) by an open labeled, prospective, and randomized clinical trial (RCT) in IHH patients in a single center of the Obstetrics and Gynecology Hospital Affiliated to Fudan University. The onset of patients' mental and psychological diseases such as depression and anxiety rely on their reproductive needs and pregnancy outcomes, which will also be investigated in the current study. Moreover, the effect of clinical interventions to improve pregnancy outcomes and emotional disorders would be discussed.

Study Timeline

• Study Start: 2021-01-01
• Study First Submitted: 2022-10-02
• Study First Submitted QC: 2022-10-05
• Study First Posted: 2022-10-06
• Status Verified: 2024-08
• Last Update Submitted: 2024-08-06
• Last Update Posted: 2024-08-07
• Primary Completion: 2025-12-31
• Study Completion: 2025-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: Female
• Target Recruitment: 46

Inclusion Criteria

• Clinical diagnosis of IHH (primary amenorrhea (with or without a history of hormone supplementation therapy); basic LH levels <5IU/L, FSH<5IU/L or normal; no organic lesions in the hypothalamus and pituitary MRI).
• Women of childbearing age who desire to get pregnant

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Exclusion Criteria

• Premature ovarian insufficiency or premature ovarian failure
• Primary amenorrhea due to hypothalamic/pituitary lesions
• Secondary amenorrhea

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Additional hCG injection	Additional hCG injection	An additional hCG injection of 2000-5000IU would be performed 48 hours following routine hCG trigger on the basis of supplementation of estrogen and dydrogesterone in IHH patients.
No additional hCG injection	estrogen and dydrogesterone	Only estrogen and dydrogesterone would be given for luteal phase support in IHH patients.
Additional hCG injection	estrogen and dydrogesterone	An additional hCG injection of 2000-5000IU would be performed 48 hours following routine hCG trigger on the basis of supplementation of estrogen and dydrogesterone in IHH patients.

Primary Outcome Measures

Name	Time	Method
Clinical pregnancy rate	7 weeks	Defined as the presence of a gestational sac under ultrasonography
Live birth rate	42 weeks or beyond	Defined as the number of deliveries that resulted in a live born neonate, expressed per 100 pregnancies.
Cumulative pregnancy rate	12 weeks	Defined as a pregnancy with a detectable heart rate at 12 weeks of gestation or beyond.

Secondary Outcome Measures

Name	Time	Method
Number of IHH patients with ovarian hyperstimulation syndrome	12 weeks or beyond	Ovarian hyperstimulation syndrome is defined as an exaggerated response to excess hormones. It usually occurs in women taking injectable hormone medications to stimulate the development of eggs in the ovaries. Ovarian hyperstimulation syndrome (OHSS) causes the ovaries to swell and become painful.
Number of IHH patients ending in early pregnancy loss	12 weeks	Early pregnancy loss is defined as the loss of a pregnancy prior to 12 weeks gestation

Trial Locations

Locations (2)

OB & GYN Hospital of Fudan University; 🇨🇳 Shanghai, Shanghai, China

Obstetrics and Gynecology Hospital of Fudan University; 🇨🇳 Shanghai, Shanghai, China