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Percutaneous uterine electrical signal acquisition and database establishment during pregnancy and delivery

Percutaneous uterine electrical signal acquisition and database establishment during pregnancy and delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071122
Enrollment
Unknown
Registered
2023-05-05
Start date
2023-05-08
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

uterine contraction

Interventions

Sponsors

Women’s Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) Desire for vaginal delivery; 2) single pregnant women; 3) Age =18 years old; 4) 20 weeks of gestation to labor; 5) Participate voluntarily and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) The presence of uterine deformity, uterine scar, severe uterine myoma or adenomyosis; 2) Allergic to alcohol or ECG electrode patches; 3) Patients who are participating in other clinical studies; 4) Researchers believe that other reasons are not suitable for clinical researchers (high-risk patients with pregnancy complications or complications such as pregnancy induced hypertension, high-risk premature delivery patients with recurrent vaginitis, patients with appendicitis and cholecystitis after conservative treatment in the early pregnancy, etc.).

Design outcomes

Primary

MeasureTime frame
bioelectricity signal;

Secondary

MeasureTime frame
uterine contraction;pregnancy outcome;

Countries

China

Contacts

Public ContactJunhua Shen

Women’s Hospital, Zhejiang University School of Medicine

yysjh2006@126.com+86 13675810891

Outcome results

None listed

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