Normal delivery. Supervision of normal pregnancy
Conditions
Interventions
Intervention 1: In controls group, normal saline was injected subcutaneously in sacrum area. Intervention 2: In cases group distilled water was injected subcutaneously in sacrum area.
Placebo
Treatment - Drugs
In controls group, normal saline was injected subcutaneously in sacrum area
In cases group distilled water was injected subcutaneously in sacrum area.
Sponsors
Birjand University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: term pregnancy, alive fetus and active phase of labour. Exclusion criteria: preterm labour; fetal death; labour inducton (oxcytocin prostaglandin) and use of sedatives
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: At the begging of the study and minutes: 40, 60 and 90. Method of measurement: Visual analogue scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Demand for sedative. Timepoint: At the end of the study. Method of measurement: Questionaire.;Patient satisfaction from treatment. Timepoint: At the end of the study. Method of measurement: Questionaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Nahid Ghanbarzadeh
Birjand University of Medical Sciences
Outcome results
None listed