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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05271188
Other study ID # Pain control
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 15, 2022
Est. completion date March 2023

Study information

Verified date March 2022
Source Assiut University
Contact Salwa Hussein
Phone 01159460234
Email salwa94hussien@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A comparison between IPACK block and adductor canal block in post operative pain management


Description:

Two groups of patients between 40 and 60 yrs who are undergoing open wedge high tibeal osteotomy Group 1 will receive IPACK block with 15 ml Bupivacaine, immediately before spinal anaesthesia . Group 2 will receive adductor canal block ,also with 15 ml Bupivacaine. before spinal anaesthesia. register the time of first pain sensation and firs IV analgesic dose required in each group


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date March 2023
Est. primary completion date February 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria: 1. Age 40 - 60 years. 2. American Society of Anesthiologist class ( ASA) I - III 3. BMI 18-35 kg/m2 4. Scheduled for primary unilateral open wedge high tibial osteotomy Exclusion Criteria: 1. Known allergy to local anesthetics 2. Contraindication to local anesthetics injection e.g. infection at the site of injection 3. Contraindication to spinal anesthesia e.g. coagulopathy. 4. Patients with pre-existing motor or sensory deficits in lower extremities. 5. Insulin or noninsulin dependent diabetes mellitus. 6. systemic corticosteroid use within 30-days of surgery 7. difficulties in comprehending visual analog scale (VAS) pain scores 8. history of arrhythmia or seizures 9. severe renal insufficiency

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Infiltration of local anaesthetic between popliteal artery and posterior knee capsule
Adductor canal block (ACB) is a popular peripheral nerve block that has been shown to decrease pain significantly and thereby opioid consumption with minimal effect on quadriceps function [8]. Though ACB provides analgesia to the peripatellar and intra-articular aspect of knee joint, it does not relieve posterior knee pain which is moderate to severe in intensity [9, 10]. The recent technique of an ultrasound (US)-guided local anesthetic infiltration of the interspace between popliteal artery and the capsule of posterior knee (IPACK) has shown to provide significant posterior knee analgesia without affecting the common peroneal nerve (CPN) [11]. We postulated that IPACK will provide better pain relief and improve knee function in the immediate postoperative period compared to ACB

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary the time of first pain sensation requiring analgesia If intervention which is adductor canal block or lPACK block is effective in postoperative pain control that can decrease the lV analgesic agents 24 hours
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