Comparison of intravenous and nebulised routes of dexmedetomidine as premedication on surgical field visualisation in functional endoscopic sinus surgeries : a randomised control trial
Not Applicable
Completed
- Conditions
- Health Condition 1: J01- Acute sinusitisHealth Condition 2: J31- Chronic rhinitis, nasopharyngitisand pharyngitisHealth Condition 3: J32- Chronic sinusitisHealth Condition 4: O- Medical and SurgicalHealth Condition 5: J33- Nasal polypHealth Condition 6: J34- Other and unspecified disorders ofnose and nasal sinusesHealth Condition 7: J30- Vasomotor and allergic rhinitis
- Registration Number
- CTRI/2023/05/052754
- Lead Sponsor
- All India Institute of Medical Sciences, Bathinda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 114
Inclusion Criteria
American society of anaesthesiologists physical status 1 to 2
scheduled for elective functional endosocopic sinus surgeries under general anaesthesia
Exclusion Criteria
1. Patients not giving consent
2. Patient with body mass index = 35 kg/m2.
3. Pregnant patients
4. Patients who are allergic to any study drug
5. Patients with moderate-severe cardiovascular, respiratory, renal or hepatic impairment.
• Patients with anticipated difficult airway
• Patients who are smokers (more than 10 pack-years)
• Patients with bleeding diathesis
• Patients taking any type of BP controlling drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Surgical field visualisationTimepoint: till the end of surgery
- Secondary Outcome Measures
Name Time Method Hemodynamic changes, post-operative sore throat, post- <br/ ><br>operative nausea & vomiting and sedative effect will be observedTimepoint: till 24 hours after <br/ ><br> <br/ ><br>the end of the surgery.