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Comparison of two different block of pain carrying nerve fibres for postoperative pain management in patients with fractures of face

Comparative study of Ropivacaine with dexamethasone and Ropivacaine with dexmedetomidine for post-operative analgesia following Ultrasound guided Suprazygomatic Maxillary Nerve Block in patients undergoing nasal and maxillofascial surgeries under general anaesthesia: A prospective randomized double-blinded trial - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099479
Enrollment
60
Registered
2025-12-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: S024- Fracture of malar, maxillary and zygoma bones

Interventions

Intervention1: Ropivacaine with dexamethasone: Ultrasound guided Suprazygomatic Nerve Block Group 1: receiving the block under all aseptic precautions placing patients in supine position with face tur

Sponsors

Sir Sunderlal Hospital, IMS, BHU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age between 18 to 60 years 2) ASA PS I and II 3) Diagnosed with nasal/ zygomatic/ maxilla bone fracture requiring surgical repair

Exclusion criteria

Exclusion criteria: 1) Known allergy/hypersensitivity to the drugs used in the study 2) Head injury 3) Coagulopathy 4) Infection at the site of block 5) Pregnancy/ lactating mother 6)

Design outcomes

Primary

MeasureTime frame
Comparision of post operative analgesia over the first 24 hours after Ultrasound guided Zuprazygomatic Nerve Block with Ropivacaine plus demedetomidine versus Ropivacaine plus dexamethasoneTimepoint: VAS score at 0,1,2,3,4,5,6,12,18,24 hours after the completion of surgery—

Secondary

MeasureTime frame
1) Duration of analgesia 2) Need of rescue analgesia required in no. of doses (tramadol 2 mg/kg) in the postoperative period 3) Sedation level using Ramsay sedation scoreTimepoint: VAS score at 0,1,2,3,4,5,6,12,18,24 hours after the completion of surgery—

Countries

India

Contacts

Public ContactDr Logesh Vaibhavw VV

IMS BHU

atulksingh84@gmail.com08317010317

Outcome results

None listed

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