Effect of auricular stimulation with moxibustion paste on preoperative sleep quality, anxiety state and postoperative recovery quality of patients with surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100051062

Enrollment

Unknown

Registered

2021-09-11

Start date

2021-09-15

Completion date

Unknown

Last updated

2022-05-16

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

Conditions

preoperative anxiety

Interventions

control group:none

experimental group:moxibustion

Eligibility

Sex/Gender

Female

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Female patients aged 20-60 years; 2. ASA classification is I-II; 3. Scheduled thyroid surgery under general anesthesia; 4. Agree to use an analgesic pump.

Exclusion criteria

Exclusion criteria: 1. Suffering from any chronic disease, vision or hearing impairment; 2. Have a history of mental illness; 3. No literacy skills; 4. No mobile phone; 5. General anesthesia within 6 months; 6. Difficult airway; 7. Low patient compliance; 8. Patients with day surgery; 9. The patient has experienced allergic reactions to moxibustion or moxibustion stickers in the past.

Design outcomes

Primary

Measure	Time frame
State Anxiety Inventory;	—

Countries

China

Contacts

Public ContactWang Maohua

The Affiliated Hospital of Southwest Medical University

541067731@qq.com+86 18989131360

Outcome results

None listed

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