A randomized controlled study for the predictive model of cervical cerclage and perioperative treatment strategy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000030157

Enrollment

Unknown

Registered

2020-02-24

Start date

2020-03-01

Completion date

Unknown

Last updated

2020-02-25

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

Conditions

cervical incompetence

Interventions

experimental group:cervix cerclage

control group:conservative treatment

blank control group:no intervention

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients were included if they had viable singleton pregnancies and had indications for cerclage placement which diagnosed by ACOG Cerclage for the Management of Cervical Insufficiency.

Exclusion criteria

Exclusion criteria: Patients were excluded if the fetus had known structural or chromosomal abnormalities, or if the patient had experienced persistent contractions, vaginal bleeding, premature rupture of membranes and clinical symptoms or laboratory findings suggestive of chorioamnionitis.

Design outcomes

Primary

Measure	Time frame
Pregnancy outcomes;Neonatal outcome;	—

Countries

China

Contacts

Public ContactMian Pan

panmian1973@126.com+86 13178031273

Outcome results

None listed

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