Regional Anesthesia in TKA: Impact on Postoperative Joint Motion and Patient Satisfaction

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKonya City Hospital

About this trial

This is a single-center, prospective, randomized controlled trial aiming to evaluate the effects of different regional anesthesia/analgesia techniques on postoperative knee range of motion (ROM) and patient satisfaction following total knee arthroplasty (TKA). Ninety patients undergoing elective TKA under spinal anesthesia will be randomly assigned to one of three groups: 1) spinal anesthesia with epidural catheter, 2) spinal anesthesia followed by adductor canal catheterization, and 3) spinal anesthesia with multimodal intravenous analgesia. The primary outcome is postoperative knee joint ROM measured on postoperative days 1, 2, and 3. Secondary outcomes include patient satisfaction, Oxford Knee Score, postoperative opioid consumption, and VAS scores. The study is conducted at Konya City Hospital and will be completed over a 6-month period.

Eligibility criteria

Qualifiers

Minimum Age: 18 Years

Maximum Age: None

Sex: All

Gender Based: No

Disqualifiers

Skin infection at the planned injection site

Sepsis

Coagulopathy

Refusal of neuraxial anesthesia

Trial design

Treatments tested in this trial

  • Regional anethesia

Treatment groups

30 Participants
are divided into 3 treatment groups

Sponsors and collaborators