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Recruiting NCT07526831

NCT07526831 Comparison of the Analgesic Efficacy of Adductor Canal Block and Combined Adductor Canal Block Plus IPACK Block in Knee Surgery

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Clinical Trial Summary
NCT ID NCT07526831
Status Recruiting
Phase
Sponsor TC Erciyes University
Condition Knee Arthroplasty, Total
Study Type OBSERVATIONAL
Enrollment 60 participants
Start Date 2026-04-15
Primary Completion 2028-04-15

Trial Parameters

Condition Knee Arthroplasty, Total
Sponsor TC Erciyes University
Study Type OBSERVATIONAL
Phase N/A
Enrollment 60
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2026-04-15
Completion 2028-04-15
Interventions
Adductor Canal Block Group (Group I)Adductor Canal + iPACK Block Group (Group II)"

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Brief Summary

To evaluate the effectiveness of Adductor Canal Block and combined Adductor Canal plus IPACK block in reducing postoperative pain and analgesic requirements in patients undergoing knee surgery.

Eligibility Criteria

Inclusion Criteria: * ASA (American Society of Anesthesiologists) I- ASA II-ASA III Patients Exclusion Criteria: * history of allergy to the study medication * refusal to participate

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