Effect of sleep quality on postoperative nausea and vomiting in gynecological patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900027964

Enrollment

Unknown

Registered

2019-12-07

Start date

2019-12-31

Completion date

Unknown

Last updated

2019-12-10

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

Conditions

gynecological operation

Interventions

Case series:Nil

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. ASA classification: I-III; 3. Female, choose a time to perform gynecological operation under endoscope; 4. Total intravenous anesthesia or combined intravenous and inhalation anesthesia were used; 5. BMI 18-24kg/m2.

Exclusion criteria

Exclusion criteria: 1. Serious mental illness; 2. Combined with heart, liver, kidney, gastrointestinal and other systemic diseases; 3. Postoperative analgesia pump; 4. Patients who used antiemetic drugs or had nausea and vomiting within 24 hours before operation; 5. Smoking and motion sickness.

Design outcomes

Primary

Measure	Time frame
The level of PONV;	—

Countries

China

Contacts

Public ContactGuo Wenjun

The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital

gwj8581@sina.com+86 13605532244

Outcome results

None listed

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