A study to observe pain relief after nerve block in patients undergoing middle ear surgery
Phase 4
Completed
- Conditions
- Health Condition 1: H663- Other chronic suppurative otitis media
- Registration Number
- CTRI/2021/03/032232
- Lead Sponsor
- Government Medical College and Hospital Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 46
Inclusion Criteria
1.ASA physical status 1 and 2
2.Patients who can read Hindi or English
Exclusion Criteria
1.Patients with systemic disease belonging to ASA physical status >2
2.Patients having allergy or contraindication to drug used in present study.
3.Patients having history of substance abuse
4.Patients not able to understand VAS score
5.Pregnant and lactating mother
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maximum pain intensity as per pain out score.Timepoint: At 24 hours post operatively
- Secondary Outcome Measures
Name Time Method 1.Total dose and time to first rescue analgesia <br/ ><br>2.Haemodynamics <br/ ><br>3.VAS score <br/ ><br>4.Vertigo <br/ ><br>5.PONV <br/ ><br>6.Any other adverse effectsTimepoint: 1.5,10,15 minutes,1,4,8,12,18 and 24 hours post operatively <br/ ><br>2.5,10,15 minutes,1,4,8,12,18 and 24 hours post operatively <br/ ><br>3.5,10,15 minutes,1,4,8,12,18 and 24 hours post operatively <br/ ><br>4.5,10,15 minutes,1,4,8,12,18 and 24 hours post operatively <br/ ><br>5.5,10,15 minutes,1,4,8,12,18 and 24 hours post operatively <br/ ><br>6.5,10,15 minutes,1,4,8,12,18 and 24 hours post operatively <br/ ><br>