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Cervical Cerclage Pessary in Preventing Preterm Births

Not Applicable
Conditions
Health Condition 1: O343- Maternal care for cervical incompetence
Registration Number
CTRI/2023/07/054691
Lead Sponsor
Ziller Medical Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
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 <25 mm with or without cerclage.

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

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduce the incidence of preterm laborTimepoint: 12 weeks
Secondary Outcome Measures
NameTimeMethod
o secondary outcomesTimepoint: Not applicable
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