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

A Comparative study between ropivacaine and dexmedetomidine vs levobupivacaine and dexmedetomidine for post-operative analgesia using adductor canal block in patients undergoing total knee replacement surgeries.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031366
Enrollment
60
Registered
2021-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: Comparison between ropivacaine and dexmedetomidine vs levobupivacaine and dexmedetomidine in post operative analgesia.: A COMPARATIVE STUDY BETWEEN ROPIVACAINE AND DEXMEDETOMIDINE VS LE

Sponsors

Army Hospital Research and Referral
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: 1.American society of anestheiologists(ASA) grade 1V. 2.Age 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.

Design outcomes

Primary

MeasureTime frame
1.Time to first demand of rescue analgesia 2.Duration of analgesia 3.Rescue analgesic consumption (total in 24 hrs).Timepoint: 24 hours—

Secondary

MeasureTime frame
1.Onset and duration of motor block (if any). 2.Patient satisfaction score on a numeric scale (0-10 â??0â?? being not satisfied and â??10â?? being satisfied). 3.Incidence of complications.Timepoint: 24 hours—

Countries

India

Contacts

Public ContactMaj Manzoor Ali

Army Hospital(Research and Referral)

vrkysvrky@gmail.com9596899737

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026