Comparision of an anaesthetic drug and a nerve block to study better postoperative pain relief.

To compare the effictiveness of ultrasound guided Quadratus lumborum block using injection bupivacaine and intravenous tramadol for postoperative analgesia in unilateral renal surgeries- A randomised comparative study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/086596

Enrollment

Registered

2025-05-08

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil Intervention5: Quadratus lumborum block using injection Bupivacaine: At the end of surgery and before ex

Eligibility

Inclusion criteria

Inclusion criteria: Informed consent, Physical status ASA I, II, III and age group between 18 to 65 years

Exclusion criteria

Exclusion criteria: Patient refusal, Any contraindications to regional anaesthesia and those who are allergic to local anaesthesia, Patients with coagulation abnormalities, obese patients with BMI more than 29.9 kg/m2.

Design outcomes

Primary

Measure	Time frame
To compare the duration of postoperative analgesia in two groups.Timepoint: To compare the duration of postoperative analgesia in two groups upto 24 hours at different time intervals.	—

Secondary

Measure	Time frame
To compare the total consumption of analgesia in the first 24 hours.Timepoint: Total analgesic requirement in both groups will be monitored upto 24 hours postoperatively at different time intervals depending on patient complaints.;To assess complications or side effects if any.Timepoint: To assess for complications like nausea, vomiting, hypotension, bradycardia if any within 24 hours postoperatively any time if they occur within 24 hours.	—

Measure

Time frame

To compare the total consumption of analgesia in the first 24 hours.Timepoint: Total analgesic requirement in both groups will be monitored upto 24 hours postoperatively at different time intervals depending on patient complaints.;To assess complications or side effects if any.Timepoint: To assess for complications like nausea, vomiting, hypotension, bradycardia if any within 24 hours postoperatively any time if they occur within 24 hours.

—

Countries

India

Contacts

Public ContactDr Deepali Valecha

Department of Anaesthesiology, Mahatma Gandhi Memorial Medical College and M.Y.Hospital, Indore.

deepalisidhwani@gmail.com9424405405

Outcome results

None listed

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