Comparison between the success rate of standard method vs dose-dependent ovarian electrocautery in polycystic ovary syndrome

Comparison between the success rate of standard method vs dose-dependent ovarian electrocautery in patients with Polycystic ovary syndrome

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20171210037820N1

Enrollment

Registered

2018-01-02

Start date

2017-12-22

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

Infertility. Female infertility associated with anovulation

Interventions

Intervention 1: Intervention group: dose-dependent ovarian electrocautery. Intervention 2: Control group: standard ovarian electrocautery.

Treatment - Surgery

Intervention group: dose-dependent ovarian electrocautery

Control group: standard ovarian electrocautery

Eligibility

Sex/Gender

Female

Age

18 Years to 38 Years

Inclusion criteria

Inclusion criteria: Age: 18-38, Infertile women (duration more than 2 year) with polycystic ovarian syndrome cause of infertility: disorder of ovulation Normal semen analysis in partner Normal hystrosalpangography and laparoscopy Interested for participation Resistance to Clomiphene citrate

Exclusion criteria

Exclusion criteria: Other cause of infertility

Design outcomes

Primary

Measure	Time frame
Ovulation rate or pregnancy. Timepoint: every month up to 6 months. Method of measurement: Observing ovulation signs in serial transvaginal sonography or pregnancy.;Measuring progesterone level at 21th day of menstrual cycle. Timepoint: 21th day of first menstrual cycle after surgery. Method of measurement: According to level (ng/ml) / ELISA (Enzyme-linked immunosorbent assay) method.;LH, testosterone, and DHEAS serum level. Timepoint: Third day of first menstrual cycle after surgery. Method of measurement: According to LH (IU/ml) and testosterone (ng/dl) and DHEAS (µg/dl) level / ELISA (Enzyme-linked immunosorbent assay) method.	—

Measure

Time frame

Ovulation rate or pregnancy. Timepoint: every month up to 6 months. Method of measurement: Observing ovulation signs in serial transvaginal sonography or pregnancy.;Measuring progesterone level at 21th day of menstrual cycle. Timepoint: 21th day of first menstrual cycle after surgery. Method of measurement: According to level (ng/ml) / ELISA (Enzyme-linked immunosorbent assay) method.;LH, testosterone, and DHEAS serum level. Timepoint: Third day of first menstrual cycle after surgery. Method of measurement: According to LH (IU/ml) and testosterone (ng/dl) and DHEAS (µg/dl) level / ELISA (Enzyme-linked immunosorbent assay) method.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeili Hafizi

Mashhad University of Medical Sciences

hafizil@mums.ac.ir+98 51 3854 3031

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 19, 2026