CompletedNot Applicable

Comparision of IPACK and Periarticular Block With Adductor Block Alone After Total Knee Artroplasty

Turkey (Türkiye)105 participantsStarted 2021-06-22

Plain-language summary

105 patients ASA I-III, undergoing total knee arthroplasty under spinal anesthesia, will be randomly assigned into one of three groups, namely group A (n=35), where an adductor canal block, group B (N:35) where an adductor canal block with IPCAK, and group C (n=35) where an adductor canal block with PAI will be performed preoperatively. All patients will receive a standardized multimodal approach. NRS scores will be evaluated in static and dynamic conditions during the first 48 hours postoperatively.

Who can participate

Age range18 Years – 85 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Physical status according to American Society of Anesthesiologists (ASA) I-III * Patients scheduled for total knee arthroplasty Exclusion Criteria: * Previous operation on same knee * Hepatic or renal insufficiency * Younger than 18 years old and older than 85 * Patients undergoing general anesthesia * Allergy or intolerance to one of the study medications * BMI \> 40 * ASA IV * Chronic gabapentin/pregabalin use (regular use for longer than 3 months) * Chronic opioid use (taking opioids for longer than 3 months, or daily oral morphine equivalent of \>5mg/day for one month)

What they're measuring

NRS scores

Timeframe: 48 hours

Trial details

NCT IDNCT04931966

SponsorKaraman Training and Research Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-08-08

View on ClinicalTrials.gov More Osteo Arthritis Knee trials