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To study labour analgesia with drotavarin and water block

A randomized controlled study for labour analgesia using drotavarin and waterblock

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021125
Enrollment
105
Registered
2019-09-09
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: Water Block: sterile water 0.125 to 0.25 ml given intracutaneously at PSIS and 1 cm medial and inferior to it on both sides repeated at an interval of 1 - 2 hour Control Intervention1:

Sponsors

DEPARTMENT OF ANESTHESIOLOGY AND CRITICAL CARE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1] Primi and multigravida 2] Full term singleton pregnancy with established labour pain 3] Vertex presentation 4] Patient with active phase of labour

Exclusion criteria

Exclusion criteria: 1] Scarred uterus 2] Foetal demise 3] Foetal distress 4] Multiple pregnancy 5] Malpresentations 6] Cephalopelvic disproportions 7] Medical complications like heart disease, diabetes mellitus, asthma, myasthenia gravis, glaucoma psychotic illness or epilepsy

Design outcomes

Primary

MeasureTime frame
Patientâ??s satisfaction in terms of PATIENTâ??S SATISFACTION SCORE and Degree of pain relief in Labour [NRS score] Timepoint: 8 weeks

Secondary

MeasureTime frame
Duration of stages of labour APGAR score Incidence of instrumentation/aid for normal vaginal delivery Any other adverse effects on the mother and the foetus Timepoint: 8 weeks

Countries

India

Contacts

Public ContactSAYEKA MUBIN

JAWAHARLAL NEHRU MEDICAL COLLEGE, A.M.U., ALIGARH

shahlahaleem@yahoo.co.in9997448172

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 14, 2026