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OpenTrials
Completed

NCT Number: NCT05483621

Hormonal Stimulation of Spermatogenesis

Urologists and reproductive specialists are often challenged when facing patients with severe male infertility scenarios. In particular, the treatment of men with NOA demands a deeper insight. In such cases, .

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Key information

Age range

19 year–72 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Urology department - faculty of medicine, South Valley university

Qina, Egypt

About this study

The hormonal stimulation of spermatogenesis is still being explored. Thus, there is still little knowledge regarding the type of patient who might benefit from medical treatment, the optimal medication,

the regimen, and the duration of treatment. In male infertility, the induction for treatment with follicle stimulating hormone (FSH) in the induction and maintenance of spermatogenesis in patient with hypogonadotopic hypogonaism. As these patients are normally azoospermic without gonadotropin stimulation and during testosterone therapy

The presence of high numbers of progressively motile and normally formed sperms in the ejaculate during exogenous gonadotropin therapy might result in the desired clinical pregnancy for many infertile couples on an experimental basis and in some places already in clinical routine. FSH preparation are also used for treatment of normogonadotopic infertile men with idiopathic impairment of spermatogemesis.

Pulstile GnRH or exogenous gonadotropins are usually used to induce spermatogenesis and promote testicular enlargement .The regimen for gonadotropin replacement includes an initial use of human chorionic gonadotropin (HCG) for 6 to 12 months and then addition of FSH or human menopausal gonadotropins (HMG) until pregnancy

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Men with primary infertility due to non-obstructive azoospermia in two seminal analysis

Exclusion criteria

  • Patients with non-obstructive azoospermia with normal or low level of FSH.
  • Patients with serum testosterone lower than 3 nmol/L.

Treatment and study plan

Beta-hCG

Drug

Treatment of spermatogenesis

Primary outcomes

  1. Hormonal treatment

    Time frame: from baseline up to 3 months after the treatment day.

    About 100 participants receiving Beta HCG (5000 IU I.M) twice weekly to evaluate the effect of hormonal stimulation for patients with non-obstructive azoospermia

Sponsors and collaborators

Lead sponsor

Egymedicalpedia

Industry

Registry information

Official study title

Hormonal Stimulation of Spermatogenesis in Non-obstructive Azoospermia

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Aug 2, 2022
Registry last updated
Oct 19, 2023

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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