Clinical Trials Directory

Trials / Unknown

UnknownNCT05910281

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

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

Status
Unknown
Phase
Study type
Observational
Enrollment
150 (estimated)
Sponsor
Gulhane Training and Research Hospital · Other Government
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Timeline

Start date
2023-07-01
Primary completion
2024-12-01
Completion
2025-12-01
First posted
2023-06-18
Last updated
2023-07-24

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05910281. Inclusion in this directory is not an endorsement.