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Methylation haplotype index based non-invasive early screen for preeclampsia

Methylation haplotype index based non-invasive early screen for preeclampsia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034979
Enrollment
Unknown
Registered
2020-07-26
Start date
2020-08-31
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

preeclampsia/eclampsia

Interventions

Gold Standard:Clinical outcome
Index test:MELODY kit

Sponsors

Sichuan University West China Second University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years, normal understanding ability, no learning difficulties or mental illness; 2. informed and written consent; 3. live fetus at 11-14 weeks of gestation; 4. singleton pregnancies.

Exclusion criteria

Exclusion criteria: 1. Women with uterine abnormality 2. Women with HIV, HBV,HCV or Treponema pallidum positive 3. Women with benign or malignant tumors during pregnancy (except for physiological ovarian cysts and/or single uterine fibroids under the serous membrane (diameter<5cm)) 4. Women with chemotherapy or radiotherapy history 5. Women taking aspirin or other non-steroidal anti-inflammatory drugs or women took aspirin or other non-steroidal anti-inflammatory drugs within 28 days before enrolment 6. Women with chronic heart diseases or liver failure, kidney failure, respiratory failure, epilepsy, infectious gynecological diseases 7. Women with blood transfusion history within four weeks before enrolment 8. Women with history of organ transplantation, allogeneic cell therapy or stem cell therapy 9. Pregnancies complicated by major fetal abnormality identified at the 11-13 weeks assessment 10. Participation of other drug clinical trials within 3 months before enrolment 11. other conditions that clinical investigators think will decrease the quality of clinical trial

Design outcomes

Primary

MeasureTime frame
Blood Pressure;urinary protein;renal and liver function;blood coagulation function;fetal growth restriction;

Secondary

MeasureTime frame
preterm;OGTT;HbA1C;thyroid function;Apgar Score;

Countries

China

Contacts

Public ContactXinghui LIU

West China Second University Hospital, Sichuan University

xinghuiliu@163.com+86 13881883798

Outcome results

None listed

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