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Effect of four treatment protocols upon pregnancy outcome in frozen-thawed embryo transfer cycle.

assessment of the best luteal phase support (comparison of four protocols) for patients undergoing frozen-thawed embryo transfer in artificial cycle.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014082510210N3
Enrollment
280
Registered
2015-02-14
Start date
2014-12-16
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

luteal phase. Other specified conditions associated with female genital organs and menstrual cycle

Interventions

Intervention 1: control group : received cyclogest vaginal suppository twice a day for luteal phase support. Intervention 2: intervention group 1: patients who received didrogesteron oral tablet 10mg
Treatment - Drugs
control group : received cyclogest vaginal suppository twice a day for luteal phase support
intervention group 1: patients who received didrogesteron oral tablet 10mg twice a day.
intervention group2: patients who received didrogesteron oral tablet 10mg twice a day in combination with 3 dose of Amp Dipherelin 0.1mg in days of embryo transfer,(3 day,6 day )
intervention group3: patients who received didrogesteron oral tablet 10mg twice a day in combination with 3 dose of Amp HCG 1500u in days of embryo transfer,(3 day,6 day)

Sponsors

Vice chancellor for research of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: unexplained infertility ? tubal factor? mild male factor ? POF ? sub fertility in pco field ? average age between 20-40? normal uterine cavity exclusion criteria: women over 40 year? endometriosis stage III ?IV? Hydro salpinx ? severe male factor? ab normal uterine cavity ? failed embryo transfer cycle =3

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy rate. Timepoint: 6 week gestation. Method of measurement: vaginal sonogeraphy trans.

Secondary

MeasureTime frame
Ongoing pregnancy rate,Abortion rate. Timepoint: 12 week gestation. Method of measurement: vaginal sonogeraphy trans.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr parastoo soheil

Shiraz University of Medical Sciences

Parastoosoheil@yahoo.com s.kharati@yahoo.com+98 71 3227 9715

Outcome results

None listed

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