Result of Bilateral Intranasal Transmucosal Sphenopalatine Ganglion Block for Postoperative pain in Functional Endoscopic Sinus Surgery.A Randomised Placebo Control Study

Effect of Bilateral Intranasal Transmucosal Sphenopalatine Ganglion Block for Postoperative Analgesia in Funtional Endoscopic Sinus Surgery:A Randomised Placebo Control Study. - Nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/072327

Enrollment

Registered

2024-08-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: 3- Administration Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: O.5% Bupivacaine: A 10cm long sterile swab will be soaked in 3ml of 0.5% Bupivacaine and placed there for 10 minutes Intervention2: Inj 0.5% Bupivacaine: A 10cm long sterile swab will b

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adults aged 18 to 65years posted for elective functional endoscopic sinus surgery 2. ASA CLASS 1 and 2

Exclusion criteria

Exclusion criteria: 1. Patients with nasal deformities 2. Patients allergic to local anaesthetics 3. Patients with bleeding disorders 4. Patients with pregnancy

Design outcomes

Primary

Measure	Time frame
Time to request first rescue analgesic in postoperative period according to VAS scoreTimepoint: Post operative analgesia will be assessed using VAS score and if VAS score is greater than 3 then rescue analgesic in the form of Inj Tramadol 50mg IV will be given for next 24 hours	—

Secondary

Measure	Time frame
To assess hemodynamic parameters which includes Blood Pressure Heart Rate SpO2 Mean Arterial Pressure during intraoperative periodTimepoint: Baseline & every 15 minutes after induction will be assessed;To determine total rescue analgesic consumptionTimepoint: If VAS score is greater than 3 then rescue analgesic in the form of Inj Tramadol 50mg IV will be given for 24 hours;To document any complications of the block in intraoperative & postoperative periodTimepoint: Any complications will be noted;To note the total consumption of Fentanyl in intraoperative periodTimepoint: If heart rate raises greater than 20 percent of baseline then bolus dose of Inj Fentanyl 0.5mcg per kg will be given;To note total consumption of antihypertensives in intraoperative periodTimepoint: Inj Nitroglycerin & Inj Metoprolol will be used in this study	—

Measure

Time frame

To assess hemodynamic parameters which includes Blood Pressure Heart Rate SpO2 Mean Arterial Pressure during intraoperative periodTimepoint: Baseline & every 15 minutes after induction will be assessed;To determine total rescue analgesic consumptionTimepoint: If VAS score is greater than 3 then rescue analgesic in the form of Inj Tramadol 50mg IV will be given for 24 hours;To document any complications of the block in intraoperative & postoperative periodTimepoint: Any complications will be noted;To note the total consumption of Fentanyl in intraoperative periodTimepoint: If heart rate raises greater than 20 percent of baseline then bolus dose of Inj Fentanyl 0.5mcg per kg will be given;To note total consumption of antihypertensives in intraoperative periodTimepoint: Inj Nitroglycerin & Inj Metoprolol will be used in this study

—

Countries

India

Contacts

Public ContactDR Namita Arora

ABVIMS AND DR RML HOSPITAL NEW DELHI

drnamitaarora@gmail.com9868219619

Outcome results

None listed

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