Quality of recovery in patients receiving two anesthesia techniques TIVA and conscious sedatio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/04/051949
- Lead Sponsor
- HAMDARD INSTITUTE OF MEDICAL SCIENCES AND RESEARCH HAHC HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients of age 18-65 years, BMI 18.5-30,ASA 1 or 2, posted for middle ear surgeries will
be included in the study
Exclusion Criteria
Patients with baseline heart rate less than 60 beats per minute.
Patients with impaired mental status.
Patients hard of hearing and does not understand Hindi or English Language.
Patients with known allergy to local anesthetics or any of the study drugs.
Patients with the history of chronic use of analgesics, sedatives, alcohol or drug abuse.
Patients will also be excluded if operations are redo, the expected surgery time is more than
2hrs, or development of intra operative severe pain that mandates the conversion to general
anesthesia. (in case of conscious sedation).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to measure and compare quality of recovery in patients undergoing middle ear surgeries under conscious sedation and total interavenous anesthesiaTimepoint: Compare quality of recovery
- Secondary Outcome Measures
Name Time Method TO MEASURE AND COMPARE THE SURGEON SATISFACTION SCORE , OVERALL SURGICAL FIELD , INTRA OPERATIVE HEMODYNAMIC STABILITY , LENGTH OF STAY IN PACU , INCIDENCE OF POST OP NAUSEA AND VOMITINGTimepoint: IN PREOPERATIVE PERIOD AND 24 HOURS AFTER SURGERY <br/ ><br>