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A comparative study of short agonist protocol versus progestin primed ovarian stimulation protocol among egg donors at Federal Medical Centre Abuja.

A comparative study of short agonist protocol versus progestin primed ovarian stimulation protocol among egg donors at Federal Medical Centre Abuja.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202603898245344
Enrollment
211
Registered
2026-03-30
Start date
2024-04-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Pregnancy and Childbirth Fertility-female

Interventions

medroxyprogesterone acetate

Sponsors

Ogonnaya Chinasa Obire
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: )EGG DONOR: 1)Women aged between 21 and 27 years. 2)Normal hormonal screening. 3) BMI 21 to 25kg/m2 4) Serology Negative 5)No previous ovarian surgery. 6)No ovarian cysts. 7)Adequate ovarian reserve as determined by serum FSH level on day 3 of the menstrual cycle of <12mlU/ml. 8)Written informed consent obtained. B)RECIPIENT: 1)Women aged =35 years, except those with premature ovarian failure (After 35, the risk of aneuploidy, diminished ovarian reserve, and poor oocyte quality rises significantly, making them the group most likely to benefit from donor oocytes). 2)Patients with premature ovarian failure at any age. 2)Infertility diagnosis with normal uterine cavity. 3)Written informed consent obtained.

Exclusion criteria

Exclusion criteria: 1. Known chromosomal abnormalities in either partners or the egg donor. 2. Previous ovarian surgery or radiotherapy. 3. Known autoimmune or endocrine disorders. 4. Severe medical or psychiatric conditions that would preclude IVF treatment. 5. Unable to give informed consent or comply with study protocol.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure was the number of oocytes retrieved.

Secondary

MeasureTime frame
. Secondary outcomes included the duration of ovarian stimulation in days, the incidence of cycle cancellation, the fertilisation rate, the clinical pregnancy rate, and Ovarian hyperstimulation syndrome (OHSS).

Countries

Nigeria

Contacts

Public ContactEkweani John

Supervisor

johananie@gmail.com+2349050002987

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Jun 29, 2026