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Role of testosterone supplementation in poor responders on IVF outcome

Role of transdermal Testosterone gel pretreatment in poor responders on IVF outcome- A prospective randomised controlled trial with active control

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/10/010113
Enrollment
70
Registered
2017-10-16
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N979- Female infertility, unspecified Health Condition 2: null- Patients undergoing Invitro fertilisation

Interventions

Intervention1: Transdermal Testosterone gel (Androgel from Besins Health care India Pvt Ltd.): Transdermal Testosterone gel (Androgel from Besins Health care India Pvt Ltd.) 12.5 mg

Sponsors

Besins Healthcare India Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients from whom 1.FSH 2.Normal TSH, Prolactin, hepatic and renal function 3.Normal uterine cavity as assessed by Hysteroscopy and 3D USG 4.None having taken any fertility medication like gonadotropins or clomiphene in the past 3 months. 5.Patients willing to participate in the trial

Exclusion criteria

Exclusion criteria: 1.Women with known causes of decreased ovarian reserve like endometriosis grade 3 or higher 2.Women with pre-existing comorbidities like uncontrolled Diabetes, Hypertension and other chronic diseases like Chronic liver or kidney disease 3.Women with known autoimmune disorders like SLE, Autoimmune hemolytic anemia 4.Abnormal parental karyotype Abnormal Uterine cavity such as thin endometrium, severe Adenomyosis 5.Women not willing to participate

Design outcomes

Primary

MeasureTime frame
Number of oocytes retrieved per cycleTimepoint: Number of oocytes retrieved per cycle

Secondary

MeasureTime frame
To compare between 2 groups 1.Total dose and number of days of administration of Gonadotrophins ï?· Cycle cancellation rate 2.Fertilization rate 3.Cleavage rate 4.Number of good quality embryos 5.Biochemical pregnancy 6.Implantation rate 7.Clinical pregnancy rate 8.Ongoing pregnancy Rate 9.Pregnancy wastage or nonviable pregnancyTimepoint: To compare between 2 groups 1.Total dose and number of days of administration of Gonadotrophins ï?· Cycle cancellation rate 2.Fertilization rate 3.Cleavage rate 4.Number of good quality embryos 5.Biochemical pregnancy 6.Implantation rate 7.Clinical pregnancy rate 8.Ongoing pregnancy Rate 9.Pregnancy wastage or nonviable pregnancy

Countries

India

Contacts

Public ContactDr Neeta Singh

All India Institute of Medical Sciences, New Delhi

ppadmashri@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026