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A real-world pragmatic research and application demonstration on the effectiveness of a combined traditional Chinese and Western medicine based clinical decision support system for the prevention and treatment of preeclampsia

A real-world pragmatic research and application demonstration on the effectiveness of a combined traditional Chinese and Western medicine based clinical decision support system for the prevention and treatment of preeclampsia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070241
Enrollment
Unknown
Registered
2023-04-06
Start date
2023-04-29
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Preeclampsia

Interventions

CDSS group:CDSS guides basic therapy
control group:According to clinical routine diagnosis and treatment

Sponsors

Guangxi Zhuang Autonomous Region People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Carry out regular pregnancy tests in the People's Hospital of Guangxi Zhuang Autonomous Region; 2. Age 18 and above; 3. Enrollment time is before 16 weeks of pregnancy; 4. No serious complications during pregnancy.

Exclusion criteria

Exclusion criteria: 1. Poor compliance, unwilling to accept all examinations necessary for pregnancy examination; 2. Pregnant women with a history of aspirin allergy were excluded.

Design outcomes

Primary

MeasureTime frame
Incidence rate of preeclampsia;—

Secondary

MeasureTime frame
Preeclampsia related complications;Preeclampsia onset gestational week;Severity of preeclampsia onset;—

Countries

China

Contacts

Public ContactMa Yinyao

Guangxi Zhuang Autonomous Region People's Hospital

26032182@qq.com+86 182 6089 0572

Outcome results

None listed

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