Skip to content

Testing a Nerve Stimulation Device Compared to a Fake Device to Reduce Labor Pain in Pregnant Women During Early Childbirth

he Efficacy of Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Relief During First Stage of Labor- A single blinded randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096282
Enrollment
64
Registered
2025-10-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: TENS device: Participants in the intervention group will receive TENS therapy using a portable battery-operated device. Two pairs of flat electrodes (5 x 9 cm) will be placed paraverteb

Sponsors

Dr Paritosh Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Primigravida Women 2. Singleton pregnancy 3. Gestational Age more than equal to 37 weeks 4. Cephalic Presentation 5. Women in active first stage of labour with (where in active labour is defined as cervical dilatation more than equal to 4cm with adequate uterine contractions)

Exclusion criteria

Exclusion criteria: 1. Pregnancies with Medical complications such as heart disease, renal disease, psychiatric disease, seizure disorders 2. Antepartum haemorrhage 3. Cephalopelvic disproportion 4. Precipitate labour 5. Previous history of caesarean section or myomectomy 6. Women who received any other method of analgesia before entering to study. 7. Skin lesion at the site of application of TENS patch

Design outcomes

Primary

MeasureTime frame
Pain index and percentage of pain relief before and after the interventionTimepoint: during the first stage of labour (20 hours)

Secondary

MeasureTime frame
Duration of first stage of labour Mode of delivery Neonatal outcome: APGAR score at birth & at 5 minutes Need for resuscitation NICU admissions Any side effects- rashes at the site Patient satisfaction Timepoint: during first stage of labour 20 hours max

Countries

India

Contacts

Public ContactDr Paritosh Gupta

AIIMS Raipur

drsaritaagrawal@aiimsraipur.edu.in08518881744

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026