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Cervical Cerclage Pessary in Preventing Preterm Births

Prevention of Preterm Birth in Pregnant Women with Short Cervix using a Cervical Cerclage Pessary - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054691
Enrollment
60
Registered
2023-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: O343- Maternal care for cervical incompetence

Interventions

Intervention1: Pessary: Cervical cerclage pessary. Dose not applicable, one number of pessary. Route of administration through Vaginal Insertion. Duration of Intervention is 12 weeks. Control Interven

Sponsors

Ziller Medical Inc.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women who have had one or more preterm deliveries and/or mid-trimester losses with or without cerclage. Women with a cervical length Women who present with exposed membranes prolapsing through the cervical os with less than 4cm with or without cerclage. Pregnant women of all races and ethnic groups are eligible for this study.

Exclusion criteria

Exclusion criteria: Individuals who were not willing to participate in the study. Patients who were undergoing emergency interventions. Patients with chorioamnionitis, preterm prelabour rupture of membranes (PPROM), severe contractions, anatomic deviations

Design outcomes

Primary

MeasureTime frame
Reduce the incidence of preterm laborTimepoint: 12 weeks—

Secondary

MeasureTime frame
No secondary outcomesTimepoint: Not applicable—

Countries

India

Contacts

Public ContactPadmashri Parimalam

A4 Hospital and Maternity Centre

ppadmashri@gmail.com7639473035

Outcome results

None listed

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