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to compare 2 ultrasound based nerve blocks for patients who undergo elective ear surgery

Comparison of ultrasound guided lesser occipital & greater auricular nerve block (LOGAB) versus superficial cervical plexus block for postoperative analgesia in adults undergoing elective mastoid surgery under general anaesthesia: A randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/098221
Enrollment
75
Registered
2025-11-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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: LOGAB Block: Patient will receive ultrasound guided LOGAB block with 5 ml of 0.25% ropivacaine 5 minutes after induction of general anaesthesia Intervention2: SCB Block: Patient will re

Sponsors

Self
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for elective mastoid surgery 2.ASA I-II patients

Exclusion criteria

Exclusion criteria: 1. Presence of local infection or impaired skin integrity at the injection site 2. Any cognitive or psychiatric condition that prevents comprehension and completing the outcome measures 3. Patients receiving anticoagulant therapy 4. Pregnancy or breastfeeding 5. Previous neck surgery or radiation

Design outcomes

Primary

MeasureTime frame
To compare the postoperative pain intensity (by Numerical Rating Scale) between the groups.Timepoint: Baseline, 0,5,10,15,30,45,60,75,90,105,120,135,150,165,180,195,210 minutes

Secondary

MeasureTime frame
To compare the intraoperative hemodynamic profile between the groups (HR, SBP, DBP and MAP) at various time points.Timepoint: 0,5,10,15,30,45,60,75,90,105,120,135,150,165,180,195,210 minutes;To compare the time to demand of first rescue analgesia and the total dose of rescue analgesia in first 48 hours post operatively between the groupsTimepoint: post operative period;To note any adverse events such as allergic reactions, local anaesthetic toxicity, infection, hematoma, Horner s syndrome and phrenic nerve palsyTimepoint: in post operative period 48 hours;To assess the quality of recovery of the patient using the QoR-15 score in the postoperative period.Timepoint: in post operative period 48 hours

Countries

India

Contacts

Public ContactDr Ravneet Kaur Gill

Dr B R Ambedkar State Institute of Medical Sciences

drravneetkgill@gmail.com9501988361

Outcome results

None listed

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