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Effect of prophylactic noise isolation during laparoscopic surgery for postoperative pain

Effect of prophylactic noise isolation during laparoscopic surgery for postoperative pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097844
Enrollment
Unknown
Registered
2025-02-26
Start date
2025-03-07
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative pain

Interventions

Intervention group :Wear noise-cancelling earphones
Control group:None

Sponsors

General Hospital of Eastern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age of 18–70 years; 2.Elective laparoscopic surgery conducted under general anesthesia;American Society of Anesthesiologists (ASA) classification I–III; 3.American Society of Anesthesiologists (ASA) classification I–III; 4.Voluntary administration of patient-controlled intravenous analgesia (PCIA)

Exclusion criteria

Exclusion criteria: 1. Hearing abnormalities 2. History of mental illness or long-term use of such drugs 3. History of chronic pain or long-term use of analgesic medications 4. Mechanical ventilation is required after surgery or there is still a need for anesthesia 5. Those who are admitted to the intensive care unit after surgery 6. Clinical participants who have participated or are participating in other psychological intervention studies 7. Those who are unable to complete postoperative information collection 8. Received other surgeries 30 days before surgery 9. Those who are allergic to the materials contained in the headphones 10. Those who refuse informed consent

Design outcomes

Primary

MeasureTime frame
The maximum movement-evoked pain score within 72 h post-surgery;

Secondary

MeasureTime frame
The maximum resting pain score within 72 h post-surgery;The maximum movement-evoked pain score within 48 h post-surgery;The maximum resting pain score within 48 h post-surgery;Total opioid consumption over 24 h post-surgery (calculated as morphine-equivalent doses combined with doses from the PCIA pump and any additional analgesics);The number of PCIA pump button presses within 48 h post-surgery;Visual Analogue Scale (VAS) when exiting the postanesthesia care unit;Incidence of postoperative cognitive dysfunction;Intraoperative electroencephalogram analysis (Sedline);

Countries

China

Contacts

Public ContactKangli Hui

General Hospital of Eastern Theater Command

2904599064@qq.com+86 177 5670 2256

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026