A study comparing the analgesic efficacy of drug fentanyl to that of a combination of cervical superficial plexus block and dexmedetomidine in patients undergoing tympanomastoidectomy surgery
Not Applicable
- Conditions
- Health Condition 1: H662- Chronic atticoantral suppurative otitis media
- Registration Number
- CTRI/2020/05/025134
- Lead Sponsor
- AIIMS Raipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age: 18 â?? 60 years of either sex
ASA Physical status I-II
Patients under going tympanomastoidectomy
Exclusion Criteria
Patient refusal
ASA Class more than 3
BMI More Than 30
Contraindication to study drugs
Hepatic renal and cardiac insufficiency
Pregnant and lactating mothers
Uncooperative patients
Patients with chronic pain on opioids
Inability to understand VAS score
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To study the analgesic efficacy of superior cervical plexus block with dexmedetomidine over fentanyl in patients undergoing tympanomastoidectomy in both intraoperative and postoperative period. <br/ ><br>2.To study the side effects and the duration of analgesia. <br/ ><br> <br/ ><br>Timepoint: 1.At baseline <br/ ><br> <br/ ><br>2.At 5 minutes <br/ ><br> <br/ ><br>3.At 10 minutes interval upto 2 hours <br/ ><br> <br/ ><br>4.Thereafter every 15 minutes interval till end of procedure <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI