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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05751109
Other study ID # 681423
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 1, 2022
Est. completion date October 1, 2023

Study information

Verified date January 2024
Source Prof. Dr. Cemil Tascioglu Education and Research Hospital Organization
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date October 1, 2023
Est. primary completion date August 16, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ipack+adduktor kanal
nerve block

Locations

Country Name City State
Turkey Onur Karaoglu Istanbul Kagithane
Turkey Rasim Onur Karaoglu Istanbul Kagithane

Sponsors (1)

Lead Sponsor Collaborator
Prof. Dr. Cemil Tascioglu Education and Research Hospital Organization

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale (VAS) evaluation for postoperative pain The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be'). 8. Hour
Secondary Visual Analogue Scale (VAS) evaluation for postoperative pain The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be'). 1. Hour
Secondary Visual Analogue Scale (VAS) evaluation for postoperative pain The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be'). 24. Hour
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