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Clinical application of remote fetal monitoring in high-risk pregnancy

Clinical application of remote fetal monitoring in high-risk pregnancy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010900
Enrollment
Unknown
Registered
2017-03-17
Start date
2017-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

High risk pregancy

Interventions

Experimental group:remote fetal heart rate monitoring
Control:Traditional minitoring

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. High risk pregant women: hypertensive disorder complicating pregnancy , gestational diabetes mellitus , intrahepatic cholestasis of pregnancy, fetal growth restriction, oligohydramnion, placenta previa, cord around neck (at least 2 cycles), senile gravida (=35 years old); 2. gestational age =32 weeks; 3. single pregnancy; 4. Agree to participate in this study and willing to sign the informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Twins or multiple births; 2. gestational age <32 weeks; 3. Normal pregnant women; 4. Critical pregant women who cannot finish the mobile remote fetal heart rate monitoring; 5. Don't want to participate in this study or quit midway.

Design outcomes

Primary

MeasureTime frame
abnormal non-stress test detection rate;the rate of asphyxia neonatorum;

Countries

China

Contacts

Public ContactSun Bo

Shenzhen Second People's Hospital

13715251001@139.com+86 13715251001

Outcome results

None listed

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