Effect of dexmedetomidine with bupivacaine in turp

Not Applicable

Completed

• Conditions: Health Condition 1: O- Medical and Surgical

• Registration Number: CTRI/2019/02/017789
• Lead Sponsor: Department of anaesthesiology Jln Medical College ajmer

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2020-01-06
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

1.Male patients between 50 to 70 years of age.

2.ASA physical status 1,2 and 3.

Exclusion Criteria

1. ASA physical status 4,5 & 6. 2. Patients refusal.3. Patients with peripheral sensorineural deficit. 4. Patients is sensitive or allergic to study medications.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of analgesiaTimepoint: Duration of study is around 1 year

Secondary Outcome Measures

Name	Time	Method
1. ASA physical status 4,5 and 6. 2. Patients refusal. 3. Patients with peripheral sensorineural deficit. 4. Patients is sensitive or allergic to study medications. 5. Patients on anticoagulants. 6. Infection at the site of of lumbar puncture. 7. Patients who are taking α2 adrenergic agonist or antagonists. 8. Pre existing severe cardiac disease, heart block/dysrhythmias. 9. Contraindications to subarachnoid block.Timepoint: Duration of study is around one year