Construction and Validation of Preoperative Anxiety Risk Prediction Model in Gynecological Day Surgery Patients

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300074121

Enrollment

Unknown

Registered

2023-07-31

Start date

2023-08-01

Completion date

Unknown

Last updated

2023-08-07

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

Conditions

Glogical benign disease

Interventions

Trail group:none

Eligibility

Sex/Gender

Female

Age

16 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1)aged 16-60 years old,(2)duration of operation <3hours,(3)liver and kidney function and electrolytes are normal before surgery,(4)intraoperative blood loss <200ml,(5)American Society of Anesthesiologists(ASA)?-?,(6)volunteer to participate in the study.

Exclusion criteria

Exclusion criteria: (1)chronic diease wrere not effectively controlled before operation,(2)language and cognitive impairment,(3) hemoglobin<80g/L,(4) have participated in other clinical trials or research,(5)patients transferred to other department for routine treatment after surgery

Design outcomes

Primary

Measure	Time frame
preoperative anxiety risk factors;Anxiety points;	—

Countries

China

Contacts

Public ContactXu Lijuan

Chengdu Women and Children's Central Hospital

740229886@qq.com+86 138 8024 5168

Outcome results

None listed

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