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Comparing the duration of effect of Ropivacaine with Fentanyl and Ropivacaine with Dexmedetomidine for postoperative pain relief in lumbar spine surgery

Phase 4
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/10/058443
Lead Sponsor
Kathramoni Mahitha Rani
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patients undergoing elective lumbar spinal surgeries under general anaesthesia.

2. ASA grades I & II.

3. Patients willing to give informed consent

Exclusion Criteria

1. Patients receiving chronic analgesic therapy

2. Patients with history of opioid dependence

3. Patients with bleeding disorders

4. Patients on anticoagulative medication

5. Patients who refused to consent

Study & Design

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