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The effect of sphenopalatine ganglion block of both sides using ultrasound in alleviating pain of sinus surgery done using endoscope in comparison to those without block

Analgesic efficacy of USG-guided bilateral sphenopalatine ganglion block versus no block in Endoscopic Sinus Surgery: A randomized control trial - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074509
Enrollment
58
Registered
2024-09-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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 Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Bilateral SPGB: After anaesthetising the patient, SPG blockade will be performed using ultrasound via suprazygomatic approach and 4 mL of 0.5% bupivacaine and 0.5 mcg/kg bodyweight dexm

Sponsors

AIIMS Patna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA I and II 2. Patients between the ages of 18-60 years 3. Duration of surgery less than 3 hrs 4. Male and female 5. BMI 18-30kg/m2

Exclusion criteria

Exclusion criteria: 1. History of severe liver, renal or cardiovascular disease or chronic pain disease 2. Pre-existing neurological or psychiatric illness 3. Any bleeding abnormality 4. Diagnosis of allergy to the study drug 5. Sensitivity to NSAIDs 6. History of alcohol or drug abuse 7. History of chronic use of analgesics, sedatives, opioids, or steroids 8. Pregnancy 9. patients who would not want to participate in the study 10. uncooperative (due to dementia, mental retardation, etc.)

Design outcomes

Primary

MeasureTime frame
Postoperative opioid requirement will be recordedTimepoint: At 24 h postoperatively (Total opioid consumed till 24 h after surgery will be recorded)

Secondary

MeasureTime frame
Hemodynamic parametersTimepoint: 0, 1, 2, 6 & 24 h after surgery;NRS ScoresTimepoint: At 1, 2, 6 & 24 h after surgery;Time to first rescue analgesiaTimepoint: The time at which the patient first complains of pain in the postoperative period;To compare the total intraoperative opioid consumptionTimepoint: At the time of completion of surgery

Countries

India

Contacts

Public ContactShagufta Naaz

AIIMS Patna

drshaguftanaaz@gmail.com7765937919

Outcome results

None listed

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