Last updated: December 22, 2021
Sponsor: Near East University, Turkey
Overall Status: Completed
Phase
N/A
Condition
Acute Pain
Treatment
N/AClinical Study ID
NCT05169138
2021/1367
Ages 18-35 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
INCLUSİON CRİTERİA:
- Single pregnancy
- Primiparous gestational age more than 36 weeks (term)
- Cervical dilatation of at least 3 cm
- Pregnants with 3 uterine contractions in a 10-minute period lasting at least 30seconds
- Cephalic presentation
- Not receiving analgesics, sedatives or anesthetics during labor,
- Not using induction at birth
Exclusion
EXCLUSİON CRİTERİA:
- Multiparity
- cephalopelvic incompatibility
- third trimester bleeding history
- intrauterine growth retardation
- multiple pregnancy
- breech presentation
- subject's withdrawal from clinical trial
- allergy to aromatic lavender essential oil
- addiction (alcohol, smoking)
- obstetric conditions requiring emergency cesarean section
- infertility history
- previous history of diagnosis of an underlying disease
- induction at birth
Study Design
Total Participants: 121
Study Start date:
January 01, 2021
Estimated Completion Date:
November 01, 2021
Study Description
Connect with a study center
Near East University / Turkish Republic of Northern Cyprus
Nicosia,
CyprusSite Not Available

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