Comparison of Epidural Analgesia With Intra-Articular Infiltration Analgesia

StatusCompleted
PhaseNot applicable
Started

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Record History

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  1. Notable Primary completion date changed from estimate of Sep 28, 2025 to Apr 15, 2026 Show 4 more changesShow less
    • Completed without a posted recruiting period
    • Start date changed from estimate of Mar 28, 2025 to Apr 15, 2025
    • Eligibility criteria expanded, about 7 words
    • Publications: details revised at 2 of 2 entries
  2. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
The results of combining infiltrative analgesia applied by orthopedists with epidural analgesia applied by anesthesiologists after knee replacement surgery will be compared. It aims to compare epidural analgesia with the maximum reduction of postoperative pain in patients, as well as in terms of both analgesic and complications. The study will include patients who have undergone knee replacement surgery for six months. In the study, we will compare the results of painkillers applied to the patient from the waist or knee after the waist numbing anesthesia, which includes some of the routinely applied protocols of your knee replacement surgery. It is a condition that will be monitored after surgery. The study aims to reduce maximum pain with two painkiller methods applied in small amounts or together. No interventional application will be made to the patient who will undergo surgery other than routine application. After the surgery, you will be asked verbally about your pain level and side effects at certain hours after the surgery and the amount of painkillers used and the amount of painkillers will be determined according to the follow-up hours (1st, 2nd, 6th, 12th, 24th and 48th hours after the surgery). In addition to these, complications will also be monitored. The results of patients who can be fully followed up at the end of 6 months will be presented as a scientific study.
Trial Details
NCT Number NCT06872528
Lead Sponsor Namik Kemal University
Conditions
(from sponsor)
Epidural; Analgesia, Local Infiltration
Related terms Agnosia
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov