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Effect of music therapy on recovery quality after general anesthesia in female patients undergoing elective surgery

Effect of music therapy on recovery quality after general anesthesia in female patients undergoing elective surgery

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048417
Enrollment
Unknown
Registered
2021-07-06
Start date
2021-07-06
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

None listed

Interventions

Music group:light music
Control group:null

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective laparoscopic abdominal surgery under general anesthesia will be placed in the PACU with a tube after surgery; 2. ASA I-II level; 3. aged 18 to 65 years, female; 4. BMI 18.5 to 30; 5. High school education level or above; 6. To be a musician after inquiries before surgery; 7. Patients with expected operation time of 1-6 hours; 8. Voluntarily participate in this clinical trial and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Combined with severe cardiovascular and cerebrovascular diseases, severe chronic obstructive pulmonary emphysema, liver and kidney insufficiency; 2. Those who have a history of mental illness in the past; 3. Those who have a history of long-term use of psychotropic drugs; 4. History of drug use; 5. Take hypnotic sedative drugs before surgery; 6. Patients with past medical history cannot wear headphones; 7. The resting electrocardiogram is obviously abnormal during the screening period, and the investigators judge that they are not suitable to participate in the experiment; 8. Hypertensive patients who have not been satisfactorily controlled (sitting systolic blood pressure >= 160mmHg during screening, and/or diastolic blood pressure >= 105 mmHg during screening); 9. Sitting systolic blood pressure <= 90mmHg during the screening period; 10. Participated in any drug clinical trials within 30 days; 11. Other reasons that the investigator considers inappropriate to participate in the trial (such as long-term or recent hormone therapy, etc.).

Design outcomes

Primary

MeasureTime frame
Quality of postoperative recovery related scale;

Secondary

MeasureTime frame
Vital signs;Choking cough;Riker sedation agitation score;Pain visual analogue scale;The biochemical indicators;Hormone;Discomfort;

Countries

China

Contacts

Public ContactZhang Yuwen, Liu Jianhui

Shanghai Tongji Hospital

tongjiwen1984712@163.com+86 13661452939

Outcome results

None listed

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