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

G

Gulhane Training and Research Hospital

Status

Enrolling

Conditions

Postoperative Complications
Postoperative Pain
Postoperative Nausea and Vomiting

Study type

Observational

Funder types

Other

Identifiers

NCT05910281
E2-23-4135

Details and patient eligibility

About

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

Full 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.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Central trial contact

Bilal Katipoglu

Data sourced from clinicaltrials.gov

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