Skip to content

Study on the effect of wheat germ on postpartum after pain

Study on the effect of wheat germ on postpartum after pain in women that referred to Mahdieh hospital in Tehran

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200211046452N1
Enrollment
90
Registered
2020-04-01
Start date
2019-09-22
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

After Pain. Complications predominantly related to the puerperium

Interventions

Intervention 1: Intervention group: Two hours after delivery one wheat germ capsule containing 500 mg of powder will be given every six hours for 48 hours and one hour after each intervention, if the

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Be Iranian Speak Persian Lives with her husband The mother had vaginal delivery Single and healthy baby Gestational age between 37 to 42 weeks The mother has the ability to breast-feed The baby has the ability to breast-feed The mother is satisfied to participate in the study The mother suffers from moderate to severe postpartum pain Delivery whit out devices The mother has no history of cesarean section and abdominal and pelvic surgery Not used of epidural or spinal anesthesia Non-smoking and drug abuse The mother does not have a chronic disease (Hypertension, diabetes, heart disease) Has no history of allergy to wheat germ or other herbal drugs

Exclusion criteria

Exclusion criteria: Use other herbal or chemical drugs except Mefenamic Acid during the study to relieve pain The mother is suffering from serious complications after delivery (postpartum bleeding, temperature over 39 ° C,blood pressure higher than 140/90) Breast feeding may not be possible for maternal or neonatal reasons The mother is not willing to continue her participation in the study for any reason Sensitivity to wheat germ happen during study

Design outcomes

Primary

MeasureTime frame
Severity of after pain. Timepoint: Before intervention and 1 hour after it. Method of measurement: The Mc Gill Pain Ruler.

Secondary

MeasureTime frame
Side effects of the drug. Timepoint: After the intervention. Method of measurement: Side Effects Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedighe Amir Ali Akbari

Shahid Beheshti University of Medical Sciences

asa_akbari@yahoo.com+98 21 8865 5366

Outcome results

None listed

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