A Study of comparison of postoperative analgesic effects of posterior and lateral quadratus lumborum block

Comparison of postoperative analgesic effects of posterior and lateral quadratus lumborum block under ultrasound guidance following Caesarean section deliveryâ?? A randomised controlled study.

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/02/040549

Enrollment

Registered

2022-02-23

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-01

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: POSTOPERATIVE ANALGESIC EFFECTS OF lateral and POSTERIOR QUADRATUS LUMBORUM BLOCK: POSTOPERATIVE ANALGESIC EFFECTS OF lateral and POSTERIOR QUADRATUS LUMBORUM BLOCK Under ultrasound gui

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients undergoing elective Caesarean section with ASA 2 2.Age from 24 to 40 years old 3.Weight from 50 to 70 Kg 4.Patient of normal single term pregnancy with gestation age of more 37 weeks

Exclusion criteria

Exclusion criteria: 1.Patients not willing for procedure 2.Emergency LSCS 3.Allergic to local anesthetic agent 4.Patient with ASA 3 and 4 5.Coagulopathies 6.Local infections.

Design outcomes

Primary

Measure	Time frame
Reduction in consumption of postoperative IV analgesic agent between two groups. Difference in pain score between two groups measured post operatively using visual analogue pain scaleTimepoint: Reduction in consumption of postoperative IV analgesic agent between two groups after 24 hours. Difference in pain score between two groups measured post operatively using visual analogue pain scale after 24 hours.	—

Measure

Time frame

Reduction in consumption of postoperative IV analgesic agent between two groups. Difference in pain score between two groups measured post operatively using visual analogue pain scaleTimepoint: Reduction in consumption of postoperative IV analgesic agent between two groups after 24 hours. Difference in pain score between two groups measured post operatively using visual analogue pain scale after 24 hours.

—

Secondary

Measure	Time frame
Compare the hemodynamic changes, nausea, vomiting, pruritis, urinary retentionTimepoint: Outcome is assessed immediately after surgery and up to 24 hours after surgery	—

Countries

India

Contacts

Public ContactHemapriya N

Sri Venkateshwara Medical College,

rkpuduvai@gmail.com8825778958

Outcome results

None listed

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