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To compare the efficacy of nerve block in the face as compared to pain killers given via injection in blood vessel for pain relief in patients undergoing surgery of the maxillary bone

USG guided Suprazygomatic Maxillary nerveblock vs parenteral analgesics in patients undergoing maxillary surgeries :Prospective Randomized Control Trial - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084004
Enrollment
26
Registered
2025-04-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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: Suprazygomatic maxillary nerve block: Usg guided suprazygomatic maxillary nerve block is given in patients undergoing maxillary surgeries before the surgical incision.This will be admin

Sponsors

Department of Anaesthesiology,Pain Medicine and Critical Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients posted exclusively for maxillary surgeries 2.Patients giving consent 3.ASA PS 1 and 2

Exclusion criteria

Exclusion criteria: 1.Patients with hemangioma or vascular tumours around the injection site 2.Patients with any local site infection 3.Patients with deranged coagulation profile 4.Patients with decreased IQ or Mental retardation 5.Patients with local anesthetic allergy or contraindication to any of the study drugs ââ???Patients with difficult anatomy around the injection site (eg :Tmj Ankylosis)

Design outcomes

Primary

MeasureTime frame
Total amount of intra operative analgesic requirement ( iv fentanyl -mcg/kg)in patients receiving the block compared to controls receiving parenteral analgesics .Timepoint: Till the end of surgery

Secondary

MeasureTime frame
1)Time to first rescue analgesic (iv ketorolac) (mins/hrs) 2) Post operative analgesic requirement (upto 24hrs) 3) Intra operative and post operative hemodynamics (Heart rate, Mean arterial pressure, Systolic and Diastolic Blood Pressure, Oxygen saturation) 4) Adverse events if anyTimepoint: Till 24 hours post surgery

Countries

India

Contacts

Public ContactSrujana Suryadevara

All India Institute of Medical Sciences

devalinagoswami@aiims.edu9971196699

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026