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Assessment of effect of Fenugreek seed on the insulin resistancy in the infertile women with polycystic ovarian

Assessment of addetive effect of Fenugreek seed extract on the insulin resistancy in infertile women with polycystic ovarian syndrom

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138810082924N1
Enrollment
58
Registered
2010-02-02
Start date
2007-11-26
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

Insulin resistance in infertile women with polycystic ovarian syndrome(PCOS). Other disorders of genitourinary tract

Interventions

Intervention 1: Intervention group: hydroalcholic of fenugreek seeds extract capsuls and metformin tablet (Fenugreek capsuls of 500mg twice daily and metformin tablets of 500mg three times a day for 8
Treatment - Drugs
Placebo
Intervention group: hydroalcholic of fenugreek seeds extract capsuls and metformin tablet (Fenugreek capsuls of 500mg twice daily and metformin tablets of 500mg three times a day for 8 weeks)
Control group: placebo capsuls and metformin tablet(Placebo capsuls twice daily and metformin tablets of 500mg three times a day for 8 weeks)

Sponsors

Vice chancellor for research of Mashhad University of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. female infertility,2. To have two of three criteria for PCOS( oligo/amenorrhea, clinical sign or biochemical hyperandrogenism, PCOS in sonographic view), 3. insulin resistance (FGIR<4.5), 4. FBS<200mg/dl, 5. normal function of liver and kidney(Cr<1.4mg/dl), 6. selected for ovarian stimulation. Exclusion criteria: 1.diabetes mellitus type one, hyperprolactinemia, hypothyroidism, adrenal disorder, abnormal HSG, previous medical disease (septecemia, kidney failure, congestion heart failure, gastrointestinal disorder), confound drugs to the metformin.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Insulin resistance. Timepoint: End of 8 weeks. Method of measurement: Biochemical and hormonal tests.;Fasting blood sugar (FBS). Timepoint: End of 8 weeks. Method of measurement: Biochemical test.;Golucose tolerance test of two hours (GTT). Timepoint: End of 8 weeks. Method of measurement: Biochemical test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Hassanzadeh Bashtian

Mashhad university of medical sciences

bashtian@yahoo.com; M.H.Bashtian@gmail.com+98 51 1867 4826

Outcome results

None listed

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