None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.PRIMI GRAVID WOMEN 2.SINGLE FETAL CEPHALIC PRESENTATION 3.PLANED VAGINAL DELIVERY 4.TERM PREGNANCY GREATER THAN 37 WEEKS OF PREGNANCY 5.LATENT PHASE OF THE FIRST STAGE OF LABOR WITH CERVICAL DILATION LESS THAN 5 CM 6. WILLING TO GIVE WRITTEN INFORMED CONSENT
Exclusion criteria
Exclusion criteria: 1.PRIMI GRAVID WOMEN WITH OBSTETRICAL AND NON OBSTETRICAL COMPLICATIONS 2.HAD PREVIOUS EXPERIENCE OF TENS OR ACUPUNCTURE 3.MATERNAL CUTANEOUS LESION ON THE APPLICATION SITES SUCH AS WOUND SCAR, URTICARIA, ULCERS
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Pain intensity assessed using Visual analogue scale Timepoint: 1.30 minutes,60 minutes after TENS application | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Need for conventional medical analgesia 2.Duration of labor 3.Mode of delivery 4.APGAR score at 5 minutesTimepoint: 1.Number of times analgesia required during labor and delivery . 2.Total duration of labor and delivery 3.mode of delivery 4.5 minutes | — |
Countries
India
Contacts
PRAVARA INSTITUTE OF MEDICAL SCIENCES (DU)