Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06790914

Investigation on Hyperalgesia After Thoracoscopic Lung Cancer Surgery and Effects of Flurbiprofen Axidate Combined with Noise-Cancelling Headphones Music

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

90

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating hyperalgesia, or increased sensitivity to pain, in patients undergoing thoracoscopic radical lung cancer surgery. This study aims to understand the current state and factors influencing hyperalgesia after surgery, and to evaluate how combining the drug flurbiprofen axidate with noise-cancelling earphone music during surgery may affect postoperative pain levels. The study randomly assigns patients to one of three groups: flurbiprofen axidate combined with noise-cancelling headphones playing music, flurbiprofen axidate combined with noise-cancelling headphones without music, or flurbiprofen axidate alone via drip. The drug is given 30 minutes before anesthesia, and in the headphone groups, noise-cancelling headphones are applied after anesthesia induction and worn throughout the surgery. Participants will be assessed before surgery and on the first and second days after surgery for mechanical pain threshold on the healthy arm and surgical area. Pain levels are measured using a numerical rating scale, and use of additional analgesics and patient-controlled analgesia pumps are tracked within two days after surgery. Researchers also monitor intraoperative medication use and adverse reactions like nausea or hypotension. The total duration of participation spans surgery day and two days post-surgery for outcome evaluation.

CONDITIONS

Brief 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 or older who can communicate effectively and cooperate with the trial
  • ASA grade I to III
  • Normal hearing
  • No participation in other trials within the last two months
Not Eligible

You will not qualify if you...

  • Previous history of thoracic surgery
  • History of chronic pain or any analgesic use within 48 hours before surgery
  • History of mental illness or psychiatric treatment within the past six months
  • Ear deformity or inability to wear headphones
  • Severe concurrent organ system diseases or hearing impairment
  • Incomplete data collection

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Day of surgery

Participants undergo thoracoscopic lung cancer surgery with intraoperative interventions including flurbiprofen axidate administration and use of noise-cancelling headphones with or without music during the operation.

1 surgery visit (in-person)

Post-operative Follow-up

Duration - 2 days after surgery

Participants are assessed for pain levels, analgesic use, and adverse reactions during the first two days after surgery.

3 visits (1 pre-surgery and 2 post-surgery assessments)

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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