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Effects of intraoperative noise isolation on postoperative fatigue syndrome in patients undergoing laparoscopic hysterectomy

Effects of intraoperative noise isolation on postoperative fatigue syndrome in patients undergoing laparoscopic hysterectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111189
Enrollment
Unknown
Registered
2025-10-27
Start date
2025-10-30
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Postoperative fatigue syndrome

Interventions

Noise isolation group:Noise-cancelling headphones were used for noise isolation during surgery.
Control group:None

Sponsors

The First Affiliated Hospital, University of South China
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Scheduled for laparoscopic hysterectomy, with an estimated operating time exceeding 30 minutes; 2. American Society of Anesthesiologists (ASA) physical status I–II; 3. Age 18-65 years old; 4. Voluntary to participate and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with hearing impairment; 2. Conversion from laparoscopic surgery to open surgery during the surgical procedure; 3. Patients with preoperative chronic pain or long-term use of analgesics; 4. Patients with Severe cardiac, respiratory, hepatic, or renal dysfunction; 5. History of central nervous system diseases, mental illnesses, or language communication disorders, or other factors that make communication difficult and prevent completion of the scale assessment; 6. Unable to wear headphones owing to auricular deformity or be allergic to the materials contained in the ear cups; 7. Pregnant or breastfeeding patients; 8. Participating in other clinical trials within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Postoperative fatigue syndrome;Postoperative fatigue syndrome;

Secondary

MeasureTime frame
Pain score;Postoperative opioid rescue dosages;Postoperative sleep quality;

Countries

China

Contacts

Public ContactYiheng Wang

The First Affiliated Hospital, University of South China

wyheng11@163.com+86 183 7348 2898

Outcome results

None listed

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