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Effect of fenugreek on after delivery pain

Effect of fenugreek seed capsule on after delivery pain

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201206106807N4
Enrollment
82
Registered
2012-07-25
Start date
2011-08-23
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

After pain. Postpartum care and examination

Interventions

Intervention group: Fenugreek seed.tab 900mg oral-per 6 hours for 24hours
Control group: placebo:2 starch capsule 500 mg oral per 6 hour until 24 hours
Intervention 1: Intervention group: Fenugreek seed.tab 900mg oral-per 6 hours for 24hours. Intervention 2: Control group: placebo:2 starch capsule 500 mg oral per 6 hour until 24 hours.
Treatment - Drugs

Sponsors

shahid beheshty of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-people who have normal vaginal delivery; 2- people who have after delivery pain; 3-people who are multipar; 4-people who haven't NVD with vacumm , forceps or press on fondus; 5- Those people who aren't addict; 6-people who haven't L3 0r L4 rupture of perineum during NVD; 7-people who aren’t unread; 8-people who haven't history of allergy to fenogreek or other plants; 9-those haven’t history of c/s or other abdominal surgery. Exclusion criteria: 1- Hospitalization time less than 18 hours after delivery and 2- if drugs couldn’t sedate the mother and other interventions was necessary.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
After pain. Timepoint: Before intervention & 3 or 4 times after interventiom. Method of measurement: McGill pain questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsedigheh amir ali akbari

shahid beheshty of medical sciences

asa_akbari@yahoo.com+98 21 2272 9240

Outcome results

None listed

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