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Transdermal Testosterone for Poor Responder Patients Undergoing Controlled Ovarian Stimulation Prior to IVF

W

Wolfson Medical Center (WMC)

Status and phase

Unknown
Phase 4

Conditions

Infertility, Female

Treatments

Drug: Testosterone gel

Study type

Interventional

Funder types

Other

Identifiers

NCT03078569
wolfson testosterone 1

Details and patient eligibility

About

This study evaluates the efficacy of pre- IVF treatment with transdermal testosterone to enhance ovarian response in poor responders.

a randomized controlled trial with two groups, treatment group with transdermal testosterone before IVF treatment and a control group with no treatment.

Full description

One of the major challenges of Assisted reproduction technology is treating women with low ovarian response,those women achieve very poor pregnancy rate with IVF.

in recent years there is a focus

Enrollment

30 estimated patients

Sex

Female

Ages

30 to 42 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • infertility patients undergoing ART regular menses normal function of thyroid, liver and kidney normal BMI (19.3-28.9) without use of any fertility drugs in the previous two months

Exclusion criteria

  • patients with recurrent implantations failure (3 cycles and more) previous ovarian surgery uncontrolled medical illness severe endometriosis (stage 3-4) contraindication for testosterone use

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

testosterone gel
Experimental group
Description:
testosterone gel treatment group
Treatment:
Drug: Testosterone gel
Control group
No Intervention group
Description:
without testosterone treatment

Trial contacts and locations

1

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Central trial contact

amir Mr shalev, MD; ariel Mr weissman, Proffesor

Data sourced from clinicaltrials.gov

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