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comparison of two simple tools for relatability to acute postoperative pain after caeserean delivery

Evaluation of two simple tools to predict severity of acute pain after caesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/03/018076
Enrollment
200
Registered
2019-03-13
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: 1- Obstetrics

Interventions

Control Intervention1: questionnaire regarding anticipated post operative pain: 3 questions will be asked preoperatively 1- anticipated pain on VAS 2- anxiety score on 1-10 3- anticipated analgesic re

Sponsors

Divya Gupta
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Healthy parturient 2.Uncomplicated singleton pregnancy under spinal anaesthesia

Exclusion criteria

Exclusion criteria: 1.Category 1 Emergency caesarean section 2.Documented psychiatric illness 3.History of chronic alcohol, opioid or drug abuse 4.Failure of neuraxial anaesthesia 5.Allergy to study medications •Unwilling to participate

Design outcomes

Primary

MeasureTime frame
Evoked pain on VAS scale(1-10)Timepoint: 24 hours postoperative—

Secondary

MeasureTime frame
Pain at rest Analgesics consumption in 24 hours â?¢Patient satisfaction. Timepoint: at 24 hours—

Countries

India

Contacts

Public ContactDivya Gupta

Maulana Azad Medical College and Lok Nayak Hospital

kirtinath@gmail.com9968604215

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026