NCT06265441

Comparison of Pain Relief Post Knee Arthroscopy Using IPACK + Adductor Canal Block vs. Adductor Canal Block Alone

Name: Clinical Trial NCT06265441
Creator: Ain Shams University
Keywords: Postoperative Pain, Group A will receive adductor canal block after spinal anesthesia under a high-frequency ultrasound guidance in which the adductor canal is identified and 20 ml of 0.25% bupivacaine will be injected, procedure, clinical trial, Egypt

Comparison of IPACK Block With Adductor Canal Block vs Adductor Canal Block Alone for Post Operative Analgesia Following Arthroscopic Knee Surgeries

Ain Shams University·ClinicalTrials.gov·procedureNot yet recruiting

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Study focus

Disease/Condition: Postoperative Pain
Drug/Device/Intervention: Group A will receive adductor canal block after spinal anesthesia under a high-frequency ultrasound guidance in which the adductor canal is identified and 20 ml of 0.25% bupivacaine will be injected
Study type: Interventional
Intervention type: procedure

Sponsor & location

Primary sponsor: Ain Shams University
Location: Cairo, Egypt

Timeline & enrollment

Phase: N/A
Start date: Mar 01, 2024
End date: Oct 01, 2024
Enrollment: 40 participants

Primary outcome

Assessment of pain using the visual analogue scale (VAS) upon first ambulation after 8 hours from the completion of the surgical procedure and skin closure.

Summary

In this study, the invistigators aim to compare postoperative analgesia effectiveness between combined interspace between the popliteal artery and posterior capsule of the knee block (IPACK) and Adductor canal block vs. Adductor canal block alone after Arthroscopic knee surgeries focusing on VAS score assessment at 8 hours postoperative.

ICD-10 classifications

Acute painPostoperative intestinal obstructionPain, unspecifiedDuring surgical operationDuring surgical operation

Data source

Registry: ClinicalTrials.gov
Trial ID: NCT06265441
Type: Non-Device Trial

About this record

Access comprehensive clinical trial information for NCT06265441 through Pure Global AI's free database. This phase not specified trial is sponsored by Ain Shams University and is currently Not yet recruiting. The study focuses on Postoperative Pain. Target enrollment is 40 participants.

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