Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06790914

Investigation on the Status Quo of Hyperalgesia in Patients After Thoracoscopic Operation and Study on the Effect of Intraoperative Intervention

Led by Fujian Medical University Union Hospital · Updated on 2025-01-24

90

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To explore the status quo and influencing factors of hyperpain in patients after thoracoscopic surgery, and to explore the effect of earphone sound isolation during combined operation of flurbiprofen axidate and binaural beat music played by earphone during combined operation on the intervention of hyperpain after thoracoscopic surgery.

CONDITIONS

Official Title

Investigation on the Status Quo of Hyperalgesia in Patients After Thoracoscopic Operation and Study on the Effect of Intraoperative Intervention

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients selected by the same group of surgeons to perform thoracoscopic three-hole radical resection of lung cancer
  • Patients 18 years old or older, able to communicate effectively and cooperate with clinical trials
  • ASA grade I to III
  • Normal hearing
  • Patients who have not participated in other trials in the last two months
Not Eligible

You will not qualify if you...

  • Previous history of thoracic surgery
  • History of chronic pain or any analgesic intake within 48 hours before surgery
  • History of mental illness or use of psychiatric drugs or psychological treatment in the past six months
  • Deformity of the auricle, inability to wear headphones, or inability to cooperate with the study
  • Severe concurrent organ diseases or hearing impairment
  • Incomplete data collection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Fujian Medical University Union Hospital

Fujian, Fuzhou, China, 350000

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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