labor pain. Spontaneous vertex delivery
Conditions
Interventions
Intervention 1: Intervention group: In initial study (5-4 cm dilation) labor pain intensity was determined by pain visual analogue scale. Then the client was asked to inhale rosewater in dilatation of
Treatment - Drugs
Placebo
Intervention group: In initial study (5-4 cm dilation) labor pain intensity was determined by pain visual analogue scale. Then the client was asked to inhale rosewater in dilatation of 5-7 and 8-10 cm
Placebo group: In initial study (5-4 cm dilation) labor pain intensity was determined by pain visual analogue scale. Then the client was asked to inhale water (placebo) in dilatation of 5-7 and 8-10 c
Control group: In initial study (5-4 cm dilation) labor pain intensity was determined by pain visual analogue scale. Routine care was conducted by the researcher assistant. Pain intensity was measured
Sponsors
Vice Chancellor for research of Arak University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: Nulliparous women; Gestational age of 37 weeks until 42 weeks; Singleton; Cephalic presentation; 4 to 5 cm dilation Exclusion criteria: Using other methods of pain relief during the study; Labor complications after intervention; Patient intolerance
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity Labor pain. Timepoint: before and 30 min after intervention. Method of measurement: visual analogue scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Nasrin Roozbahani
Arak University of Medical Sciences
Outcome results
None listed