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Comparing the effect of Salvia hydrangea and mefenamic acid on postpartum pain

Comparing the effect of Salvia hydrangea and mefenamic acid on postpartum pain

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190217042739N1
Enrollment
100
Registered
2019-04-07
Start date
2019-03-06
Completion date
Unknown
Last updated
2019-04-23

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 in Case group is 500 mg Salvia Hydrangea capsule that give every 6 hours Till 24 hours with a Mefenamic Acid capsule that is routine treatment.Salvia Hydrangea capsuls mad

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Being Iranian can read and write Vaginal Delivery Spontaneous Exit of Plasenta and Membranes Gestational Age Between 37-42 Week Be Complained of Moderate or Severe pain after Delivery No Instrumental Delivery or Pressure on Uterus No 3 or 4 Degree Lacerration No History of Cesarian Section or Pelvic Operation Not used any Narcotic Drug during Labor and Delivery or used Atleast 4 hours ago Not used Epidural or Spinal Anesthesia during Labor and Delivery Mother Dosent have any Drug Addiction No Maternal History of Herbal Drugs Allergy Feeding is Started and will be continued Mother age between 18-35 years Deliver a Singleton and Healthy Baby No Maternal History of Chronic Disease

Exclusion criteria

Exclusion criteria: Maternal History of Herbal Drugs Allergy 3 or 4 Degree Lacerration Maternal History of Chronic Disease History of Cesarian Section or Pelvic Operation

Design outcomes

Primary

MeasureTime frame
Severity Of After Pain. Timepoint: Before Intervention And 1 Hour After It. Method of measurement: Mc Gill Pain Ruler.

Secondary

MeasureTime frame
Drug Side Effects. Timepoint: After Intervention. Method of measurement: Side Effect Questionare.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPadideh Janati Ataii

Shahid Beheshti University of Medical Sciences

padideh.janati@sbmu.ac.ir+98 21 8865 5366

Outcome results

None listed

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