Skip to main content
Clinical Trials/IRCT201512253860N22
IRCT201512253860N22
Completed
Phase 2

Comparative assessment of effect of aromatherapy with essential oil of Peppermint and essential oil of Cloves on pain intensity and anxiety in first stage of labor on primiparous women.

vice chancellor for research of School of Nursing and Midwifery of Shahid Beheshti University of Med0 sites126 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Pain and anxiety in first stage of labor.
Sponsor
vice chancellor for research of School of Nursing and Midwifery of Shahid Beheshti University of Med
Enrollment
126
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
vice chancellor for research of School of Nursing and Midwifery of Shahid Beheshti University of Med

Eligibility Criteria

Inclusion Criteria

  • Nulliparus women of age 18 to 35 years; Gestational age between 38 to 42 week; single pregnancy with cephalic presentation; newborn weight between 2500 to 4000 gr; the onset of spontaneous contraction and dilatation 4,3 cm; body mass index ranging from 19\.8 to 26; do not have allergy to Cloves; do not have allergy to Peppermint; the mother do not have use analgesic medication during intervention or 8 hours before intervention; the mother do not have problem with the smell; without having acute and chronic psycho social problem; non\-smoking and drug abuse; without having medical disorder do not have pregnancy complications. Exclusion criteria: do not have awareness of the sensitivity of clove or peppermint; Peppermint or Clove allergy or intolerance; high blood pressure; heart disorders fetus; prolapse of the umbilical cord; placenta Abruption; delivery with devices or surgical; the patient have hidden anxiety, arrest in labor; emergency cesarean section before completing the study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Similar Trials