RecruitingNot applicableNCT07561333

Comparing ACB+IPACK and ACB+BiFeS Block Combinations for Analgesia in Total Knee Arthroplasty

Studying Catastrophic antiphospholipid syndrome

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Key facts

Sponsor
Hitit University
Principal Investigator
Guvenc DOGAN, MD
Hitit University
Intervention
ACB+IPACK Group(procedure)
Enrollment
78 enrolled
Eligibility
18-80 years · All sexes
Timeline
20252026

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07561333 on ClinicalTrials.gov

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