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NCT Number: NCT07511985

Effect of Rebound Pain on Chronic Postsurgical Pain After Total Knee Arthroplasty

This prospective observational study aims to evaluate whether rebound pain after peripheral nerve block is associated with the development of chronic postsurgical pain following elective total knee arthroplasty. Adult patients undergoing unilateral total knee arthroplasty under spinal anesthesia and receiving a peripheral nerve block as part of routine multimodal analgesia will be included. No additional intervention, drug administration, or biological sampling will be performed beyond standard clinical care.

Rebound pain will be assessed during the early postoperative period using pain diaries, numeric rating scale pain scores, and analgesic consumption records. Chronic postsurgical pain and related outcomes will be evaluated at postoperative 3 and 6 months using validated instruments assessing pain severity, neuropathic pain features, psychological status, functional outcomes, and health-related quality of life. The primary outcome is the presence of chronic postsurgical pain at 3 months after surgery. Secondary outcomes include chronic pain at 6 months, pain intensity, neuropathic pain characteristics, opioid consumption, rescue analgesic requirements, sleep disturbance, and quality-of-life measures. The study also aims to explore demographic and clinical factors associated with rebound pain and chronic postsurgical pain.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years or older
  • ASA physical status I to III
  • Scheduled for unilateral elective total knee arthroplasty
  • Planned to undergo spinal anesthesia
  • Planned to receive a peripheral nerve block as part of routine multimodal analgesia
  • Able to provide informed consent and complete study assessments

Exclusion criteria

  • Chronic opioid use (60 mg oral morphine equivalent per day or more, or use for 3 months or longer)
  • Significant neuropathy or radiculopathy
  • Bilateral or two-stage total knee arthroplasty during the same hospitalization
  • Contralateral total knee arthroplasty within the previous 6 months
  • Severe cognitive impairment or major psychiatric disorder
  • Chronic analgesic dependence

Treatment and study plan

Primary outcomes

  1. Presence of Chronic Postsurgical Pain at 3 Months

    Time frame: 3 months after surgery

    Chronic postsurgical pain will be defined as pain developing or persisting after total knee arthroplasty that is not explained by another cause. Participants with pain and at least one Brief Pain Inventory-Short Form interference item score of 3 or higher at postoperative month 3 will be considered positive for chronic postsurgical pain.

Secondary outcomes

  1. Presence of Chronic Postsurgical Pain at 6 Months assessed by Brief Pain Inventory-Short Form (BPI-SF) interference score

    Time frame: 6 months after surgery

    Presence of chronic postsurgical pain at postoperative month 6 will be assessed using the same Brief Pain Inventory-Short Form (BPI-SF)-based study definition applied at month 3: pain not explained by another cause, NRS >0, and at least one BPI-SF interference item score of 3 or higher.

  2. Pain Intensity in the Early Postoperative Period

    Time frame: 0 to 72 hours after surgery

    Pain intensity at rest and during movement will be assessed using the Numeric Rating Scale during the first 72 hours after surgery.

Study contacts

Contact information is provided by the study sponsor or research team.

Mahmut Tutar, MD

CONTACT

[email protected]

+905552723704

Sponsors and collaborators

Lead sponsor

Konya City Hospital

Other

Registry information

Official study title

Effect of Rebound Pain on Chronic Postsurgical Pain After Total Knee Arthroplasty: A Prospective Observational Study

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 6, 2026
Registry last updated
Apr 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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