Health Condition 1: M179- Osteoarthritis of knee, unspecified
Conditions
Interventions
Intervention1: iPACK (Infiltration between popletial artery and capsule of knee) block: Group I - Patients that will recieve iPACK block with 10 ml of 0.2% Ropivacaine and 20mg of Triamcinolone
Contro
Sponsors
Institute of Medical Sciences (IMS), Banaras Hindu University (BHU)
Eligibility
Inclusion criteria
Inclusion criteria: 1-Patients with knee pain of more than 3 month duration. 2-Patients aged 35 - 70 years. 3-Patients with posterior knee pain. 4-Informed consent obtained from patient . 5-Paitients with ASA grade 1-3.
Exclusion criteria
Exclusion criteria: 1-Patients with knee pain due to any lumbo - sacral spine pathology. 2- Patients with previous history of tibial or femoral fracture. 3- Patients with BMI more than 30 kg/metre suqare. 4- Patients with history of any infection or inflammation. 5- Patients who are allergic to local anaesthetic drugs. 6-Patients who decline to provide consent or withdraw from study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the effect of iPACK block on pain score - Numerical Rating Scale (NRS ) Score.Timepoint: 1. Before the procedure. 2. 2 hours after the procedure. 3. 7 days after the procedure. 4. 15 days after the procedure. 5. 30 days after the procedure. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Evaluate the effect of iPACK on functional recovery of the patient - Western Ontario and McMaster Universities Osteoarthritis Index( WOMAC Score ). 2. Monitor complications (motor weakness, sensory loss) that may occur during and after the procedure.Timepoint: 1. Before the procedure. 2. 2 hours after the procedure. 3. 7 days after the procedure. 4. 15 days after the procedure. 5. 30 days after the procedure. | — |
Countries
India
Contacts
Public ContactDr Sumita Kumari
Institue of Medical Sciences (IMS), Banaras Hindu University (BHU)
Outcome results
None listed