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Genicular Nerve Block Versus Its Combination With Infiltration Between Popliteal Artery and Capsule of Posterior Knee

Not Applicable
Recruiting
Conditions
Postoperative Pain
Interventions
Drug: standard analgesia (paracetamol and meloxicam)
Procedure: GNB plus standard analgesia
Procedure: 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
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
C groupstandard 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 groupGNB plus standard analgesiathe patients will take standard analgesia plus GNB
G groupstandard analgesia (paracetamol and meloxicam)the patients will take standard analgesia plus GNB
GI groupGNB plus IPACK block plus standard analgesiathe patients will take standard analgesia plus GNB plus IPACK
GI groupstandard analgesia (paracetamol and meloxicam)the patients will take standard analgesia plus GNB plus IPACK
Primary Outcome Measures
NameTimeMethod
2 hours visual analogue scaleat 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 scoreat 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 scoreat 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 scoreat 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 scoreat 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 scoreat 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 scoreat 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
NameTimeMethod
• Total morphine consumptionat 24 hours post-operatively

Total morphine consumption

degree of maximum active flexion and extension of the kneeat 24 hours post operative

the angle of maximum active flexion and extension of the knee

walk testat 24 hours post operative

walking distance in meters that patients can wake during 2 min

holding quadriceps muscleat 24 hours post operative

number of patients capable to hold quadriceps muscle more than 5 seconds.

• Time of performance of blockfrom 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 effectat 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

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