To observe pain relief following neck block in patients undergoing middle ear surgeries

Phase 4

Completed

• Conditions: Health Condition 1: O- Medical and Surgical

• Registration Number: CTRI/2019/02/017712
• Lead Sponsor: Department of Anaesthesiology and Intensive Care unit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-11-17
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

1. Age between 18 to 65 years of age group

2. American Society of Anaesthesiology(ASA)physical status I and II of both sex

3. Body mass index(BMI) 20 to 35kg/m2

Exclusion Criteria

1.Patients having history of alcohol abuse

2.Patients having history of PONV, motion

sickness

3.Patients receiving drugs for chronic pain

management

4.Patients having allergy or contraindications to

drugs used in present study

5.Patients having any history of migraine,

seizure

6.Patients having any history of malignancy

7.Pregnancy and lactating mothers

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction in Visual analog score(VAS)Timepoint: Postoperative at 5, 10, 15 minutes , 1, 4, 8, 12, 18, 24 hours.

Secondary Outcome Measures

Name	Time	Method
1.Haemodynamics <br/ ><br>2.Total rescue analgesia <br/ ><br>3.Time to first rescue analgesia <br/ ><br>4.Nausea/vomiting <br/ ><br>5.Vertigo <br/ ><br>6.Adverse effectsTimepoint: 1. at 5, 10, 15 minutes , 1, 4, 8, 12, 18, 24 hours. <br/ ><br> <br/ ><br>2. at 5, 10, 15 minutes , 1, 4, 8, 12, 18, 24 hours. <br/ ><br> <br/ ><br>3. at 5, 10, 15 minutes , 1, 4, 8, 12, 18, 24 hours. <br/ ><br> <br/ ><br>4. at 5, 10, 15 minutes , 1, 4, 8, 12, 18, 24 hours. <br/ ><br> <br/ ><br>5. at 5, 10, 15 minutes , 1, 4, 8, 12, 18, 24 hours. <br/ ><br> <br/ ><br>6.at 5, 10, 15 minutes , 1, 4, 8, 12, 18, 24 hours. <br/ ><br>