Comparison the efficacy of lavender aroma and valerian in reducing labor pain and Progress of labor in nulliparous wome
Not Applicable
- Conditions
- abor pain.Other specified assisted single delivery
- Registration Number
- IRCT201504236582N10
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 141
Inclusion Criteria
Inclusion Criteria: Primiparous pregnancy; age 18-35; gestational age of 37-41 w; singleton fetus; active phase; cephalic presentation; no smoking; no addiction; no Lack of vision; no history of chronic heart diseases, lung diseases, according to the patient's expression; the absence of eclampsia; and placenta previa; no PROM for more than 18 hours; no history of infertility; willingness to participate in the study; no history of sensitivity; the presence of low-risk pregnancies.
Exclusion Criteria
Get analgesic medication during the 3 hours before the start of the study; systolic blood pressure less than 95 mm Hg.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of labor pain. Timepoint: before intervention, 6-8-10cm of cervix dilatasion. Method of measurement: VAS (Visual Analog Scale).
- Secondary Outcome Measures
Name Time Method The duration of the active phase. Timepoint: each 2 hour. Method of measurement: vaginal examination.;Duration of the second stage of labor. Timepoint: from full dilatasion until lTime of Birth. Method of measurement: Questionnaire.;Neonatal outcomes (The first and fifth minute Apgar scores and Refer to the NICU). Timepoint: After birth. Method of measurement: Questionnaire.;Type of delivery. Timepoint: After birth. Method of measurement: Questionnaire.;Side effects (Nausea and vomiting). Timepoint: During the study. Method of measurement: cheklist.