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Comparison of Long protocol And Agonist-Antagonist protocol in the infertile normal responder patients

Comparison of Long protocol And Agonist-Antagonist protocol in the infertile normal responder patients undergoing ICSI cycles

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022326711N1
Enrollment
120
Registered
2016-04-11
Start date
2016-01-14
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

Infertility. Female infertility

Interventions

Intervention 1: In Agonist -Antagonist protocol in second day of cycle agonist GNRH (DECAPEPTYL0.1MG)used SC for 3 days and then gonadotropin (Gonal-f ) administered. After 6 days vaginal sonography
Treatment - Drugs
In Agonist -Antagonist protocol in second day of cycle agonist GNRH (DECAPEPTYL0.1MG)used SC for 3 days and then gonadotropin (Gonal-f ) administered. After 6 days vaginal sonography done frequently
In Long protocol in second or third day of cycle OCP started for 21 days. In Mid-luteal phase agonist GNRH (SUPERFACT) administered for 7 days and menstruation started and In second or third day of

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: normal responder infertile patients included (It means age less than 40 and normal ovarian reserve( 6AMH>1); also patients had good response to previous ovarian stimulation: BMI more than 30 . Exclusion criteria: low responder patients; high responder patients; using donated oocyte and donated egg; single ovary; endometriosis; if patient's husband need to use TESE and PESA.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Number of oocyte metaphase 2. Timepoint: After ovarian puncture. Method of measurement: Microscope- by counting oocyte.

Secondary

MeasureTime frame
Age. Timepoint: Chronological age. Method of measurement: Birth Certificate - year.;Time of infertility. Timepoint: At first. Method of measurement: Interviews with patient - year.;Type of infertility. Timepoint: At first. Method of measurement: Interviews with patient - Infertility divided in two groups: primary (no pregnancy history) and secondary.;Chemical pregnancy. Timepoint: Two weeks after transfer. Method of measurement: Blood test - bhcg titration.;Clinical pregnancy. Timepoint: Four weeks after transfer. Method of measurement: Vaginal sonography - View gestational sac and fetal heart rate.;The number of matured follicle. Timepoint: Before puncture. Method of measurement: Vaginal sonography - The number of matured oocyte with size of18mm or more.;The number of antral follicle. Timepoint: At first. Method of measurement: Vaginal sonography - The number of antral follicle with size of 2-9 mm in follicular phase.;The number of punctured oocyte. Timepoint: After puncture. Method of measurement: Microscope - The number of punctured oocyte.;The number of fetus. Timepoint: After puncture. Method of measurement: Microscope-The number of fetuses after injection.;The number of transferred fetus. Timepoint: In the time of transfer. Method of measurement: Microscope - The number of fetuses transfer in uterine.;The days stimulation. Timepoint: At first of cycle. Method of measurement: Documents - The number of days that using gonadotropin.;Endometrial thickness. Timepoint: Before transfer. Method of measurement: Vaginal sonography - mm.;BMI. Timepoint: At first. Method of measurement: Examination of patient - Dividing weight in kg by the square of one's height in cm.;The number of drug used. Timepoint: In the end of treatment. Method of measurement: Documents - The number of drugs using for ovarian stimulation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Fateme Fakhar Moghadam

Shariati Hospital, Tehran University of Medical Sciences

haniyehfm@gmail.com+98 21 2207 4679

Outcome results

None listed

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