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Comparison of the efficiency of two short- term agonist protocols with conventional long protocol in women candidate Microinjection

Comparison of the efficiency of two short- term agonist protocols with conventional long protocol in women candidate Microinjection

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201310311760N26
Enrollment
150
Registered
2014-08-02
Start date
2014-05-15
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Female infertility associated with male factors. Female infertility associated with male factors

Interventions

Intervention 1: Control Groups: Standard protocol, for Down regulation, Triptorelin dose of 0.1 (to SC) from day 21 of the cycle begins.Continues until the day of HCG injection. Gonadotropins for s
Treatment - Drugs
Control Groups: Standard protocol, for Down regulation, Triptorelin dose of 0.1 (to SC) from day 21 of the cycle begins.Continues until the day of HCG injection. Gonadotropins for stimulate ovulat
Intervention Group1: Triptorelin dose of 0.1 (to SC) from day 21 of the cycle begins. Four day, gonadotropin injection stops.
Intervention Group2: Triptorelin dose of 0.1 (to SC) from day 21 of the cycle begins. First day, gonadotropin injection stops.

Sponsors

Vice chancellor for research,Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusio criteria: Healthy women 18 to 40 years; BMI = 20-32; Regular menstrual Exclusion criteria: Women PCOs; thyroid disorders, severe endometriosis, those with ovarian or uterine and ovarian pathology; FSH> 15 IU / LI on day 3 of the cycle; POOR RESPONSE; history of hyper stimulation in previous cycles; smokers; Abnormalities of the uterus, ovary-stimulating drugs or diet 2 months ago or the diet

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pregnancy. Timepoint: 4 weeks after embryo transfer. Method of measurement: Laboratory.

Secondary

MeasureTime frame
The number of embryos. Timepoint: 14 the next day embryo transfer. Method of measurement: Ultrasound.;The number of high quality embryos. Timepoint: 14 the next day embryo transfer. Method of measurement: Ultrasound.;Total fertility/ET. Timepoint: 14 the next day embryo transfer. Method of measurement: Ultrasound.;The number of abortions performed. Timepoint: After 10 weeks of gestational sac formation. Method of measurement: clinical.;Consists of dominant follicles. Timepoint: 12 -16 day cycle. Method of measurement: Ultrasound.;Of the ampoules used per protocol. Timepoint: Duration of treatment. Method of measurement: clinical.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Poope A Rezaeian

Fatemehzahra Infertility & reproductive Health Reseach Center

persia_ph@yahoo.com+98 11 1227 4881

Outcome results

None listed

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