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Study between ropivacaine and dexmedetomidine vs levobupivacaine and dexmedetomidine in post operative analgesia in adductor canal block.

Not Applicable
Conditions
Health Condition 1: M171- Unilateral primary osteoarthritisof knee
Registration Number
CTRI/2021/02/031366
Lead Sponsor
Army Hospital Research and Referral
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Age 30-75 yrs.

2.American society of anestheiologists(ASA) grade I- III.

3.Written Informed Consent for the procedure.

Exclusion Criteria

1.American society of anestheiologists(ASA) grade 1V.

2.Age <30 and >75 yrsPatients with BMI > 30 Kg/m2 .

3.Patient refusing block.

4.Patients with known allergies to the study drugs.

5.Patient with history of psychiatric disease on psychotropic medication.

6.History of medical conditions like, bleeding diatheses and local skin site infection.

7.History of alcohol or drug abuse

8.Uncooperative patient.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Time to first demand of rescue analgesia <br/ ><br>2.Duration of analgesia <br/ ><br>3.Rescue analgesic consumption (total in 24 hrs).Timepoint: 24 hours
Secondary Outcome Measures
NameTimeMethod
1.Onset and duration of motor block (if any). <br/ ><br>2.Patient satisfaction score on a numeric scale (0-10 â??0â?? being not <br/ ><br>satisfied and â??10â?? being satisfied). <br/ ><br>3.Incidence of complications.Timepoint: 24 hours
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