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The effect of Fenugreek on sleep quality of primiparous women

The effect of Fenugreek oral capsule on sleep quality of primiparous women in the postpartum period

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230306057640N1
Enrollment
60
Registered
2023-03-14
Start date
2023-04-21
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep disorders. Sleep disorders

Interventions

Intervention 1: Intervention group: Oral capsule of Fenugreek Extract Made in the Pharmacology Department of Mashhad University of Medical Sciences, each capsule contains 700 mg of Fenugreek seed Ext

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: First delivery, age 18-35 years, singleton vaginal birth without complications, full-term pregnancy (37-40 weeks) , baby weight 2500-4000 grams, no history of medical illness, no history of mental disorders and no use of tranquilizers section, obtaining a score less than 10 in the Edinburgh test, a sleep quality score higher than 5 according to the Pittsburgh sleep quality questionnaire, no abuse of alcohol or smoking, no drug addiction, no history of depression in first-degree relatives, fenugreek allergy, breast feeding

Exclusion criteria

Exclusion criteria: Reluctance to continue the research, suffering from any disease or complication requiring hospitalization in the mother and baby, occurrence of any unfortunate incident during the study, irregular use of medicine

Design outcomes

Primary

MeasureTime frame
Sleep quality. Timepoint: Before the study and 15, 30 , 60 days postpartum. Method of measurement: Pittsburgh Sleep Quality Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Mohamadi

Mashhad University of Medical Sciences

mohammadis992@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Aug 5, 2026