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A real-world study of recurrent pregnancy loss in China-"thrombophilia" and pregnancy outcome

A real-world study of recurrent pregnancy loss in China-"thrombophilia" and pregnancy outcome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075643
Enrollment
Unknown
Registered
2023-09-11
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

recurrent miscarriage

Interventions

Recurrent miscarriage group:Pregnancy Care Management
Healthy menstruating women group:none
Healthy pregnancy group:none

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Recurrent miscarriage group: (i) presence of =2 pregnancy losses from conception to 24 weeks of gestation, (ii) 18 years = age = 40 years; Healthy menstruating women group: (i) no adverse maternal history, (ii) =1 delivery, (iii) 18 years = age = 40 years; Healthy pregnancy controls: (i) gestational status, (ii) Complete maternity information, (iii) 18 years = age = 40 years;

Exclusion criteria

Exclusion criteria: Recurrent abortion group: (i) history of thrombosis or bleeding disorders; (ii) acute infections, surgery and anticoagulant administration in the last 2 months. Healthy menstruating women group: (i) history of smoking; (ii) history of hypertension, diabetes mellitus, heart disease, chronic kidney disease, liver disease, neoplasm, and immune system disorders prior to pregnancy; (iii) acute and chronic hematologic disorders prior to or during pregnancy; (iv) anticoagulant or antiplatelet medications prior to enrollment; (v) history of recent traumas and surgeries; (vi) patients with a definitive diagnosis of antiphospholipid syndrome and a predisposition to thrombosis; (vii) a history of recurrent miscarriages; (viii) a history of thrombotic or hemorrhagic disorders; and (ix) healthy participants presenting in the second trimester with hypertensive disorders of pregnancy (HDP). Healthy pregnancy group: (i) history of smoking; (ii) history of hypertension, diabetes mellitus, heart disease, chronic kidney disease, liver disease, neoplasm, and immune system disorders prior to pregnancy; (iii) acute and chronic hematologic disorders prior to or during pregnancy; (iv) anticoagulant or antiplatelet medications prior to enrollment; (v) history of recent traumas and surgeries; (vi) patients with a definitive diagnosis of antiphospholipid syndrome and a predisposition to thrombosis; (vii) a history of recurrent miscarriages; (viii) a history of thrombotic or hemorrhagic disorders; and (ix) healthy participants presenting in the second trimester with hypertensive disorders of pregnancy (HDP).

Design outcomes

Primary

MeasureTime frame
pregnancy outcome;

Secondary

MeasureTime frame
thrombin–antithrombin III complex (TAT);plasmin-a2-plasmininhibitor complex (PIC);thrombomodulin (TM);tissue plasminogen activator–inhibitor complex(t-PAIC);

Countries

China

Contacts

Public ContactWang Fang

Lanzhou University Second Hospital

ery_fwang@lzu.edu.cn+86 139 1930 2888

Outcome results

None listed

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