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Comparison of quadratus lumborum block for postoperative analgesia after abdominal surgery

Comparison of levobupivacaine and ropivacaine in quadratus lumborum block for postoperative analgesia after abdominal surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/08/057027
Enrollment
76
Registered
2023-08-29
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

Intervention1: preoxygenated with 100% oxygen and premedicated with glycopyrolate 0.2mg kg and fentanyl 2mcg kg and anesthesia: 12 to 48hrs Control Intervention1: Incidence of nausea and vomiting: 72

Sponsors

Department of Anaesthesiology
Lead Sponsor
Department of General Surgery
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients giving written consent will be taken Patients of either sex aged 18-65 years ASA I-II patients scheduled to undergone

Exclusion criteria

Exclusion criteria: Local infection at site of block Cardiovascular disease H/o allergy to study medications known hypersensitivity to LA body mass index =35 kg/m2, =16kg/m2 history of opioid addiction bleeding diathesis renal and hepatic dysfunctions pregnancy

Design outcomes

Primary

MeasureTime frame
To study duration of analgesia i.e. time needed for first rescue analgesia in postoperative period.Timepoint: To study duration of analgesia i.e. time needed for first rescue analgesia in postoperative period.

Secondary

MeasureTime frame
Total rescue analgesic consumption in postoperative period Postoperative pain scores using the visual analog scale (VAS) for pain at rest in the postoperative period at 0, 1, 6, 12, and 24 hours. Postoperative patient’s hemodynamics by mean blood pressure and heart rate at 0, 1, 6, 12, and 24 hours. Incidence of nausea and vomiting To compare complications if any Timepoint: 24hrs

Countries

India

Contacts

Public ContactPROF REETU VERMA

King Georges Medical University Lucknow

reetuverma1998@gmail.com9473641975

Outcome results

None listed

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