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

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-08-01

Study Completion Date

2023-10-01

Brief Summary

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To compare the efficacy and complications of IPACK and adductor canal block combination and epidural block in patients who will be operated for knee arthroscopy under spinal anesthesia.

Detailed Description

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Between 15.08.2022 and 15.04.2023, the patients who will be operated on for knee surgery under spinal anesthesia, older than 18 years of age were included in the study. Demographic characteristics of the patients, comorbidities, ASA scores, mobilization time, amount of postoperative analgesic use, and postoperative pain scores of the 1. 8. 24. hours will be observed. The vas score at the 3rd month was learned over the phone.

Conditions

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Knee Injuries

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

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

Intervention Type PROCEDURE

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

Intervention Type PROCEDURE

nerve block

Interventions

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ipack+adduktor kanal

nerve block

Intervention Type PROCEDURE

Other Intervention Names

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kombine epidural

Eligibility Criteria

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Inclusion Criteria

* Those who consented to participate in the study
* 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 under the age of 18
* Patients to be operated under general anesthesia
* Disease that will cause limited cooperation
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

OTHER

Sponsor Role lead

Responsible Party

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Rasim Onur Karaoglu

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Onur Karaoglu

Istanbul, Kağıthane, Turkey (Türkiye)

Site Status

Rasim Onur Karaoglu

Istanbul, Kağıthane, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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681423

Identifier Type: -

Identifier Source: org_study_id

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