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The effect of Anethum graveolens extract on after pai

Phase 2
Conditions
after pain.
Postpartum care and examination
Registration Number
IRCT2015070623102N1
Lead Sponsor
Vice chancellor for research, Ahwaz JundiShapur University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
108
Inclusion Criteria

people who have normal vaginal delivery; people who are multipar; people who have term pregnancy; people who have after delivery pain; infant weight range is 2500-4000 g; Possible drug orally. Exclusion criteria: if drugs could not sedate the mother and other interventions was necessary; Dystocia and prolonged labor; those have history of c/s or other abdominal surgery; those have any history of postpartum hemorrhage; those have history underlying disease.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The duration of pain. Timepoint: Four times in one day. Method of measurement: Per minute.;The frequency of abnormal bleeding. Timepoint: Four times in one day. Method of measurement: The number of pads used.;The intensity of after pain. Timepoint: Four times in one day. Method of measurement: Visual pain scale.
Secondary Outcome Measures
NameTimeMethod
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