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The effect of progesterone on pregnancy rates in the intrauterine insemination cycles

The effect of progesterone suppository to luteal phase support on pregnancy rates in the intrauterine insemination cycles

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017041233379N1
Enrollment
100
Registered
2017-05-15
Start date
2017-05-22
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

Condition 1: Infertility. Condition 2: Infertility. Female infertility associated with anovulation Female infertility, unspecified

Interventions

Intervention 1: All cycles were gently stimulated after baseline transvaginal ultrasonography with 100 mg oral tablets of clomiphen citrate daily for 5 days starting on day 3 of the menstrual cycle
Treatment - Drugs
All cycles were gently stimulated after baseline transvaginal ultrasonography with 100 mg oral tablets of clomiphen citrate daily for 5 days starting on day 3 of the menstrual cycles and a sta
control group received no medicine.

Sponsors

Individual
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
No minimum to 36 Years

Inclusion criteria

Inclusion criteria: inclusion criteria:normal sonograph;normal fsh , lh @AMH;without cardiac, pulmonary and renal disease;mild endometriosis;normal sperm analysais;normal HSG and exclusion criteria:more than 36 years old;previous ovarian surgery;tubal factor;severe endometriosis; Hypothalamic Amenorrhea ;Endocrine causes of infertility and amenorrhea;patients with more than 3 Follicles with 14 mm diameters;sever oligoasthenospermia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Chemical pregnancy. Timepoint: 16 days. Method of measurement: beta HCG>50 milli-international units per milliliter (mIU/ml).;Clinical pregnancy. Timepoint: 6 weeks. Method of measurement: gestational sac in sonography.

Secondary

MeasureTime frame
Abortion. Timepoint: 20 weeks. Method of measurement: loss of pregnancy before 20 weeks.;Side effects. Timepoint: 9 months. Method of measurement: patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Yasaei Mehrjardi

Shahid Sadoughi University of Medical Science

info@ssu.ac.ir+98 35 3724 0171

Outcome results

None listed

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