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Identifying the effectiveness of addition of an opioid drug to a combination of drugs in Ultrasonography guided adductor canal block for post operative pain relief in patients undergoing knee surgeries

A prospective Randomised controlled trial to compare the efficacy of Ropivacaine and dexamethasone vs Ropivacaine and dexamethasone with buprenorphine in ultrasonography guided adductor canal block for post operative analgesia in patients undergoing knee surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063968
Enrollment
70
Registered
2024-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: M966- Fracture of bone following insertion of orthopedic implant, joint prosthesis, or bone plate Health Condition 2: M238- Other internal derangements of knee

Interventions

Intervention1: Injection Tramadol: Inj. Tramadol 50 mg will be given post operatively once patient complains of pain and VAS score is greater than 3/10 Control Intervention1: Buprenorphine: Comparing

Sponsors

SHREE KRISHNA HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with ASA (American society of Anaesthesia) I,II,III physical status 2) Patients of either sex within Age 18-75 years 3) Patients undergoing knee surgery in one or both limb.

Exclusion criteria

Exclusion criteria: 1) Allergy to local anesthetic drugs 2) Patient refusing for spinal anaesthesia 3) Local site infection. 4) Bleeding diasthesis

Design outcomes

Primary

MeasureTime frame
To compare the duration of post operative analgesia provided by addition of dexamethasone vs addition of dexamethasone and buprenorphine to ropivacaine in knee surgery patients.Timepoint: To evaluate VAS and FAS score in post operative period in a time frame of 2 hours for first 12 hours and 4 hours for next 12 hours respectively—

Secondary

MeasureTime frame
• To identify a better combination of drugs which can be used for perineural analgesia with lesser side effects . • To identify Functional assessment score (FAS Score) in both the groups. • To compare the total number of rescue analgesic needed in both the groups.Timepoint: Within 24 hours of post operative period—

Countries

India

Contacts

Public ContactDr Parth Goswami

PRAMUKH SWAMI MEDICAL COLLEGE

vaibhavih@charutarhealth.org9909977446

Outcome results

None listed

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