Skip to content

Antagonist Protocol in Poor Responders

Does the Addition of Growth Hormone to the Invitro Fertilization/ Intracytoplasmic Sperm Injection Antagonist Protocol Improve Outcome in Poor Responders? A Randomized Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02195947
Enrollment
141
Registered
2014-07-21
Start date
2014-07-31
Completion date
2015-07-31
Last updated
2021-11-11

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

Conditions

Female Infertility Due to Diminished Ovarian Reserve

Keywords

Growth hormone, IVF/ICSI, Poor responder, Antagonist protocol

Brief summary

The effect of use of the growth hormone with antagonist protocol on the outcome of the IVF/ICSI cycles in poor responders.

Detailed description

Two groups of poor responder female patients planned to receive the antagonist IVF/ICSI protocol are randomized to whether or not to add growth hormone to their protocol.

Interventions

DRUGGrowth Hormone

Growth hormone (Norditropin, Novo nordisk) was administrated on day 6 of HMG stimulation daily in a dose of 2.5 mg S.C. till the day of hCG administration.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* females fulfilling the criteria of the ESHRE consensus 2011: * at least two of the following three features must be present: * dvanced maternal age (≥40 years) or any other risk factor for POR * previous POR (≤3 oocytes with a conventional stimulation protocol) * an abnormal ovarian reserve test (i.e. AFC ,5-7 follicles or AMH ,0.5 -1.1 ng/ml).

Exclusion criteria

* women who suffer from any other cause of infertility other than poor ovarian reserve * refusal of the patient to consent for using her data in the study.

Design outcomes

Primary

MeasureTime frame
Live birth rateUp to 9 months

Secondary

MeasureTime frame
Clinical pregnancy rateUp to 5 weeks

Other

MeasureTime frame
Chemical pregnancy rate5 weeks
Early miscarriage rateUp to 12 weeks
Ongoing pregnancy rateUp to 12 weeks

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026