MedPath

The effect of rosewater on cervical ripening

Phase 3
Recruiting
Conditions
Cervical ripening.
Registration Number
IRCT20180904040952N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

Residence in Tabas city
Age between 18 to 35 years
Nulliparous women with 40 weeks gestational age
Singleton pregnancy with cephalic presentation
Bishop score less than or equal 4
Intact amniotic sac
Normal pattern of fetal heart rate
The natural number of fetal movements or reactive non-stress test
Estimated fetal weight between 2500 to 4000

Exclusion Criteria

The presence of medical and obstetric problems in the present pregnancy
Patients with previous cesarean section or hysterotomy
Placenta previa and history of third trimester hemorrhage
Pelvic examination, intercourse and stimulation of the nipple during the last 24 hours or during the study
Laxatives, herbal, chemical, or traditional methods to start a labor within the last 24 hours or during the study
Irregular consumption or non-use of rose water during one week of study
Delivery in a central location other than Tabas Hospital
Patient intolerance
Regular uterine contractions

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cervical ripening measurement. Timepoint: Before the intervention, three days and seven days after the beginning intervention. Method of measurement: Cervical Bishop score.
Secondary Outcome Measures
NameTimeMethod
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