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NCT05910281 Clinical Trial

Rebound Pain and Related Factors in Postoperative Patients With Total Knee Arthroplasty

Postoperative Pain Clinical Trial

Official title:
Rebound Pain and Related Factors in Patients Who Underwent Femoral Nerve Block for Postoperative Pain Control in Total Knee Arthroplasty

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05910281
Other study ID # E2-23-4135
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2023
Est. completion date December 1, 2025

Study information
Verified date July 2023
Source Gulhane Training and Research Hospital
Contact Bilal Katipoglu
Phone +905543330380
Email drbilal07@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The aim of this prospective observational study is to detect rebound pain and related factors in postoperative patients with total knee arthroplasty.

Description:

Total knee arthroplasty is an effective treatment method for knee osteoarthritis and because it is an invasive method, more than 50% of patients experience postoperative pain. Peripheral nerve blocks are widely used for optimal pain control. The femoral block is a frequently preferred peripheral nerve block method for postoperative analgesia in total knee arthroplasty surgery. However, after peripheral nerve block, a condition called rebound pain (rebound pain), which is described as very severe pain, lasting about 2 hours, usually of the burning type, occurs. The aim of this prospective observational study is to detect rebound pain and related factors in postoperative patients with total knee arthroplasty.

Recruitment information / eligibility
Status Recruiting
Enrollment 150
Est. completion date December 1, 2025
Est. primary completion date December 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - 18-80 years older age who underwent total knee arthroplasty Exclusion Criteria: - ASA score 4 or >4 - Active infection - End stage organ failure - Pregnancy - Established diagnosis neuropsychiatric disease ( epilepsy, neuropathy, neuromuscular disease, cerebrovascular disease...) - Uses of oral corticosteroids

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Ankara City Hospital Ankara None Selected

Sponsors (1)
Lead Sponsor Collaborator
Gulhane Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale 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'). postoperative 3-5 days fellow-up
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