Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: USG guided sphenopalatine block: Participants randomized to the intervention group will receive an ultrasound-guided sphenopalatine ganglion (SPG) block prior to functional endoscopic s
Sponsors
AIIMS Nagpur
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients aged 18 to 50 years 2. American Society of Anesthesiologists physical status I or II
Exclusion criteria
Exclusion criteria: 1. Patients aged less than 18 years and more than 50yeras 2. Emergency surgeries 3. Patient not willing to participate. 4. Patients with infective pathologies eg mucormycosis. 5. Patients with cardiac disorders. 6. History of allergy to medications being used.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of intraoperative haemodynamic stability between trans-nasal and ultrasound-guided SPG block techniques, assessed by heart rate (HR) and mean arterial pressure (MAP) measured at predefined intervals throughout surgeryTimepoint: Every 15 min throughout the surgery and upto 2 hrs postoperatively | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Outcomes:Total intraoperative opioid consumption in both groups. Requirement of additional agents (dexmedetomidine) for achieving permissive hypotension during surgery. Quality of the surgical field, assessed using the surgeon-rated Surgical Field Rating (SFR) scale. Block performance time in the ultrasound-guided group (Group U). Postoperative pain scores assessed using the VAS at predefined intervals (0, 2, 6, 12 & 24 hours). Incidence of postoperative complications within 24 hours, including headache, visual disturbances, nausea, vomiting, sore throat, & swallowing difficulty.Timepoint: At 24 hours postoperatively | — |
Countries
India
Contacts
Public ContactRidhima Sharma
AIIMS Nagpur
Outcome results
None listed