Genicular Nerve Block Versus Its Combination With Infiltration Between Popliteal Artery and Capsule of Posterior Knee
- Conditions
- Postoperative Pain
- Interventions
- Drug: standard analgesia (paracetamol and meloxicam)Procedure: GNB plus standard analgesiaProcedure: GNB plus IPACK block plus standard analgesia
- Registration Number
- NCT05672784
- Lead Sponsor
- Zagazig University
- Brief Summary
Comparison of the analgesic and physical recovery effect of genicular nerve block (GNB) alone and (GNB + infiltration between popliteal artery and posterior capsule of the knee (IPACK) in patients undergoing total knee replacement
- Detailed Description
Comparison of preemptive analgesia of (GNB) with (GNB+ IPACK) on postoperative pain control and recovery of knee physical activity in patient undergoing total knee replacement.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 63
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description C group standard analgesia (paracetamol and meloxicam) the patients will take standard analgesia ( meloxicam (15 mg) once a day + paracetamol 1gm /3 times a day). ,with no nerve block G group GNB plus standard analgesia the patients will take standard analgesia plus GNB G group standard analgesia (paracetamol and meloxicam) the patients will take standard analgesia plus GNB GI group GNB plus IPACK block plus standard analgesia the patients will take standard analgesia plus GNB plus IPACK GI group standard analgesia (paracetamol and meloxicam) the patients will take standard analgesia plus GNB plus IPACK
- Primary Outcome Measures
Name Time Method 2 hours visual analogue scale at 2 hour postoperative. pain intensity at rest and with motion using visual analogue scale from " horizontal line of 10-cm long with two ends, one end indicate no pain 0 and the other end indicate worst pain 10".
4 hours visual analogue score at 4 hours postoperative pain intensity at rest and with motion using visual analogue scale from " horizontal line of 10-cm long with two ends, one end indicate no pain 0 and the other end indicate worst pain 10".
8 hours visual analogue score at 8 hours postopertaive pain intensity at rest and with motion using visual analogue scale from " horizontal line of 10-cm long with two ends, one end indicate no pain 0 and the other end indicate worst pain 10".
18 hours visual analogue score at 18 hours postoperative pain intensity at rest and with motion using visual analogue scale from " horizontal line of 10-cm long with two ends, one end indicate no pain 0 and the other end indicate worst pain 10".
24 hours visual analogue score at 24 hours postoperative pain intensity at rest and with motion using visual analogue scale from " horizontal line of 10-cm long with two ends, one end indicate no pain 0 and the other end indicate worst pain 10".
6 hours visual analogue score at 6 hours postoperative pain intensity at rest and with motion using visual analogue scale from " horizontal line of 10-cm long with two ends, one end indicate no pain 0 and the other end indicate worst pain 10".
12 hours visual analogue score at 12 hours postoperative pain intensity at rest and with motion using visual analogue scale from " horizontal line of 10-cm long with two ends, one end indicate no pain 0 and the other end indicate worst pain 10".
- Secondary Outcome Measures
Name Time Method • Total morphine consumption at 24 hours post-operatively Total morphine consumption
degree of maximum active flexion and extension of the knee at 24 hours post operative the angle of maximum active flexion and extension of the knee
walk test at 24 hours post operative walking distance in meters that patients can wake during 2 min
holding quadriceps muscle at 24 hours post operative number of patients capable to hold quadriceps muscle more than 5 seconds.
• Time of performance of block from putting of U.S probe till the end of block procedure defined as time from putting of U.S probe till the end of block procedure.
•incidence of Anticipated side effect at 24,48 hours postoperative nausea, vomiting, itching, hemorrhage, bradycardia and hypotension.
time up and go (TUG) at 24 hours post operative the time required for the patient to stand up from a standard-height armchair, walk 3 meters, turn, walk back to the chair, and sit down
Trial Locations
- Locations (1)
Heba M Fathi
🇪🇬Zagazig, Egypt