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Growth Hormone For Poor Ovarian Reserve Patients in ICSI Trials

Effect of Growth Hormone Adjuvant Therapy on ICSI Trials For Poor Ovarian Reserve Patients

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05602090
Enrollment
120
Registered
2022-11-01
Start date
2022-02-01
Completion date
2023-10-30
Last updated
2023-04-28

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

Conditions

Poor Ovarian Reserve

Brief summary

Effect of Growth Hormone Adjuvant Therapy on ICSI Trials For Poor ovarian Reserve Patients

Detailed description

To study the effect of growth hormone as adjuvant treatment on the outcomes of ICSI trials in poor ovarian reserve patients.

Interventions

DRUG4 IU of recombinant GH (Somatotropin )

4 IU of recombinant GH

Sponsors

Beni-Suef University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

According to Bologna criteria (((at least two )))of the following features must be present: 1. Advanced maternal age (40years). 2. A previous poor ovarian response with 3 oocytes retrieved after conventional stimulation 3. An abnormal ovarian reserve test (ORT) * antral follicle count (AFC)\<7 or * anti-Müllerian hormone (AMH)\<1.1ng/ml.

Exclusion criteria

1. Any known contraindications to the approved fertility drugs. 2. Any contraindications to growth hormone, pregnancy (to be ruled out and documented before GH treatment) 4- Hydrosalpinx 5- Uterine malformations or abnormal uterine cavity. 6- Basal FSH more than 17 IU. 7- Abnormal karyotyping 8- Partner with severe male factor 9- Uncontrolled endocrinopathies: DM, hyperthyroidism, hypothyroidism.

Design outcomes

Primary

MeasureTime frameDescription
pregnancy rateICSI trial (1month)HCG positive

Countries

Egypt

Contacts

Primary ContactSara A Salem, MD
sara_abdallah100@yahoo.com01272842226

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026