Comparison of IPACK and Adductor Canal Block Combination Versus Epidural Analgesia for Total Knee Arthroplasty
NCT ID: NCT05751109
Last Updated: 2024-01-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
80 participants
OBSERVATIONAL
2022-08-01
2023-10-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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ipack+adductor canal block
The 40 patients received ACB + IPACK (Group 1, n = 40),. All patients were evaluated with VAS score for pain recorded at 1h, 8 h, postoperative day (POD) 1 and 3. month after the surgery. The secondary outcome measures assessed were movement time and discharge time.
ipack+adduktor kanal
nerve block
epidural analgesia
The 40 patients received combine spinal epidural (Group 2, n = 40),. All patients were evaluated with VAS score for pain recorded at 1h, 8 h, postoperative day (POD) 1 and 3. month after the surgery. The secondary outcome measures assessed were movement time and discharge time.
ipack+adduktor kanal
nerve block
Interventions
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ipack+adduktor kanal
nerve block
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Patients over the age of 18 who will be operated on due to knee pathology
* Patients to be operated under spinal anesthesia
* Disease that will limit cooperation
Exclusion Criteria
* Patients to be operated under general anesthesia
* Disease that will cause limited cooperation
18 Years
65 Years
ALL
Yes
Sponsors
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Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
OTHER
Responsible Party
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Rasim Onur Karaoglu
Principal Investigator
Locations
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Onur Karaoglu
Istanbul, Kağıthane, Turkey (Türkiye)
Rasim Onur Karaoglu
Istanbul, Kağıthane, Turkey (Türkiye)
Countries
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Other Identifiers
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681423
Identifier Type: -
Identifier Source: org_study_id
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