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The effect of preoperative chlorhexidine mouthwash on postoperative sleep in patients undergoing gynecological laparoscopic surgery

The effect of preoperative chlorhexidine mouthwash on postoperative sleep in patients undergoing gynecological laparoscopic surgery: A randomized clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113170
Enrollment
Unknown
Registered
2025-11-25
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

gynecological disease

Interventions

Chlorhexidine group:Use chlorhexidine mouthwash before the operation to rinse the mouth
Control group:Rinse mouth with saline solution

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Elective gynecological laparoscopic surgery under general anesthesia with an expected operation time of more than 2 hours; 2. Female patients aged 18 years or older; 3. American Society of Anesthesiologists (ASA) classification I-III; 4. BMI 18-30 kg/m^2; 5. No obvious dental caries, periodontitis, oral abscess, precancerous lesions, fungal infections, or pericoronitis of wisdom teeth in the entire mouth.

Exclusion criteria

Exclusion criteria: 1. The patient refused to participate in the study; 2. Within the past 6 months, the patient has used antibiotics or immunosuppressants systemically; 3. Within the past 6 months, the patient has a history of oral medication and surgical treatment; 4. Has been using sedatives or glucocorticoids for a long time; 5. Pregnant or lactating women; Women or men with reproductive capacity who are unwilling to use contraception throughout the study period; Or subjects who have a pregnancy plan within 3 months after the study ends; 6. Those with cognitive dysfunction or inability to communicate; 7. Allergic to chlorhexidine mouthwash; 8. With a history of alcohol or drug dependence or abuse; 9. Difficult to follow up or have poor compliance; 10. The investigator considers that there are any other factors that make the subject unsuitable to participate in this clinical study.

Design outcomes

Primary

MeasureTime frame
Oral microbiota;

Countries

China

Contacts

Public ContactLi Zhengqian

Peking University Third Hospital

liyicomeon@163.com+86 180 0129 8582

Outcome results

None listed

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