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A clinical trial to compare dexmedetomidine or propofol with combination of scalp block on hemodynamic and postoperative recovery parameter in chronic subdural hematoma surgery

Phase 4
Completed
Conditions
Health Condition 1: null- Burr hole for chronic subdural hematoma patients
Registration Number
CTRI/2015/01/005478
Lead Sponsor
Apollo Hospitals Bilaspur CG India
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

1. ASA grade I and III,

2. Scheduled for surgery under scalp block

Exclusion Criteria

1.Patients with known sensitivity to study drugs

2.Glasgow coma scale <12

3.history of drug or alcohol abuse,

4.history of chronic pain or daily intake of analgesics

5.Oral anticoagulant use (warfarin)

6.Patients with bleeding diathesis

7.impaired kidney or liver functions and

8.psychiatric patients

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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