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To study pain relief after caesarean section by ultrasound guided erector spinae plane block.

Analgesic efficacy and safety of ultrasound guided Erector spinae plane block after caesarean section -A Prospective Randomized controlled study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033746
Enrollment
44
Registered
2021-05-24
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: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: Ultrasound guided Erector spinae plane block: ultrasound guided Erector Spine plane block after caesarean section for post operative analgesia Control Intervention1: Control group to wh

Sponsors

Government Medical College Baroda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) singleton, full term pregnancy 2) ASA Physical status â?? I or II 3) scheduled for elective LSCS under spinal anesthesia

Exclusion criteria

Exclusion criteria: 1) Patients refusal and not able to understand study protocol. 2) Contraindication to spinal anesthesia. 3) Severe PIH 4) Patients with compromised renal and liver function, uncontrolled diabetes severe cardiovascular and respiratory disease. 5) Patients have allergy to any study drugs Infection, trauma, scar or sinuses at site of block 6) BMI > 35 Kg/m2 7) If patient is taken under general anaesthesia at any point of time during the course of surgery.

Design outcomes

Primary

MeasureTime frame
To compare the duration of analgesia between control nd study groupTimepoint: Visual analogue scale score will be assessed after 2 hours of Erector spinae plane block

Secondary

MeasureTime frame
1)To compare the total amount of rescue analgesia required in first 24 h post Operatively. 2. VAS scores at 2,4,6,8,12,18,24 hours. 3. Hemodynamic parameter in both groups. [PR, BP, SPO2] post block 4)complications of the technique and drugTimepoint: Baseline During procedure At 15,30,45, and 60minute. At 2,4,6,8,12,18,24hour

Countries

India

Contacts

Public ContactDr Kumud s Ganvit

Government medical college Baroda,Vadodara

drkumudsganvit@gmail.com9825607625

Outcome results

None listed

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