Labor pain. Other specified assisted single delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of labor pain. Timepoint: before intervention, 6-8-10cm of cervix dilatasion. Method of measurement: VAS (Visual Analog Scale). | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences