Comparision of Dexmedetomidine versus Midazolam and Fentanyl combination on post-operative psychomotor functions and recovery

Phase 4

Completed

• Conditions: Health Condition 1: H65-H75- Diseases of middle ear and mastoid

• Registration Number: CTRI/2021/03/032061
• Lead Sponsor: BPS Govt Medical College for Women

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2021-12-05
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 72

Inclusion Criteria

1. Patients who are willing to give written informed consent to participate in the study.

2. Patients aged between 18 and 60 years undergoing middle ear surgery done under local anesthesia.

3. Patients fit for the procedure according to Pre Anesthetic Checkup.

4. Patients who are literate at least up to 5th standard or more.

5. Patient having physical status of 1 and 2 according to American Society of Anesthesiologists

Exclusion Criteria

1. Patients who are not willing to give written informed consent.

2. Patients having a history of any neurological or psychological disease.

3. Patients who have a history of hypersensitivity to any of the study drugs or any contraindication to any drug involved in this study.

4. Patients who are taking any medicine that affects psychomotor functions.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the effect of dexmedetomidine versus midazolam & fentanyl combination on post-operative psychomotor functions after middle ear surgeries done under local anesthesiaTimepoint: Baseline psychomotor assessment and delirium assessment will be done 30 minutes prior to the shifting of patient to operation theatre and after completion of surgery both will be assessed at 1hour, 2 hour, 4 hour and 8 hour