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Postoperative pain relief after caesarean section

Efficacy of 0.2% Ropivacaine in surgeon assisted transverse abdominis plane block for postoperative analgesia after caesarean delivery (Performed under spinal anaesthesia)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/017917
Enrollment
60
Registered
2019-03-05
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: null- Asa grade II Health Condition 2: O82- Encounter for cesarean delivery without indication

Interventions

Intervention1: Transverse abdominis plane block: 0.20% Ropivacaine 20 ml each side.Duration of post-operative analgesia the time of need for the first dose of rescue analgesia (VAS â?¥ 3) will be not

Sponsors

Chandra Prakash Kalwar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient giving willful consent

Exclusion criteria

Exclusion criteria: Patient Refusal, ASA grade >II, Age 35 kg/m2, Complicated pregnancy, Patient with known hypersensitivity to local anaesthetics

Design outcomes

Primary

MeasureTime frame
Quality of AnalgesiaTimepoint: at VAS 3 or more—

Secondary

MeasureTime frame
Duration of first rescue analgesia Total dose consumption of rescue analgesia Post discharge satisfaction Adverse eventsTimepoint: 48 hours—

Countries

India

Contacts

Public ContactChandraprakash Kalwar

Rajasthan University of Health Sciences, Jaipur

khemraj10@gmail.com9414759782

Outcome results

None listed

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