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A prospective cohort study of the perioperative symptom management model of gynecological ambulatory surgery based on patient-reported outcomes

A prospective cohort study of the perioperative symptom management model of gynecological ambulatory surgery based on patient-reported outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092838
Enrollment
Unknown
Registered
2024-11-25
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Gynecologic disease

Interventions

Use the Patient Report Outcome Symptoms management platform and set up an early warning:None
Use the Patient Report Outcome Symptoms management platform and not set up an early warning:None

Sponsors

The Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) The patient has good compliance and agrees to participate in this clinical study with informed consent; (2) The American Association of Anesthesiologists (American Society of Anesthesiologists, ASA) grade I-II had no obvious cardiopulmonary disease, and grade III co-morbidities were stable for more than 3 months; (3) Meet the indications for gynecological day surgery; (4) Ensure adult companionship within after departure.

Exclusion criteria

Exclusion criteria: (1)Sexual behavior occurred 3 days before surgery; (2)Body temperature was> 37.5?; (3)Acute and subacute reproductive tract serious inflammation, such as vaginitis, acute cervicitis, endometritis, pelvic inflammatory disease, etc.;(4) No recovery from acute upper respiratory tract infection or asthma attack and persistent status;(5) Acute phase of heart, liver and kidney failure and other patients who cannot tolerate surgery; (6)Recent (within 3 months) history of uterine perforation or uterine surgery; (7)Suffering from serious mental illness or mental illness;(8) Severe coagulation dysfunction.

Design outcomes

Primary

MeasureTime frame
Postoperative symptoms of gynecological day surgery;

Secondary

MeasureTime frame
Anxiety state;

Countries

China

Contacts

Public ContactYuhua Zeng

The Affiliated Hospital of North Sichuan Medical College

2742796290@qq.com+86 817 259 8273

Outcome results

None listed

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