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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02708264
Other study ID # 214/2015
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2016
Est. completion date March 2021

Study information

Verified date November 2018
Source Federico II University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Spontaneous preterm birth (SPTB) remains the number one cause of perinatal mortality in many countries, including the United States. Multiple gestations are at increased risk of SPTB. A short cervical length (CL) on transvaginal ultrasound (TVU) has been shown to be a good predictor of SPTB, in both singletons and twins.

The cervical pessary is a silicone device that has been used to prevent SPTB. The efficacy of the cervical pessary has been assessed in several populations including singletons with short CL, unselected twins, twins with short CL, and triplet pregnancies. Several randomized clinical trials (RCTs) have been published, and several are ongoing. However, no consensus on use of the cervical pessary in pregnancy or guidelines for management have been assessed.


Recruitment information / eligibility

Status Recruiting
Enrollment 242
Est. completion date March 2021
Est. primary completion date January 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- 18-50 years of age

- Twin pregnancy (limits the participants to female gender)

- Short cervical length (less than or equal to 30 mm) on second trimester ultrasound at 18-23 6/7 weeks gestation

Exclusion Criteria:

- Singleton or higher order than twins multiple gestation

- Monoamniotic twins

- Twin twin transfusion syndrome

- Ruptured membranes

- Lethal fetal structural anomaly

- Fetal chromosomal abnormality

- Cerclage in place (or planned placement)

- Vaginal bleeding

- Suspicion of chorioamnionitis

- Ballooning of membranes outside the cervix into the vagina

- Painful regular uterine contractions

- Labor

- Placenta previa

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Cervical pessary
The cervical pessary is a silicone device that has been used to prevent SPTB

Locations

Country Name City State
Italy Gabriele Saccone Napoli

Sponsors (1)

Lead Sponsor Collaborator
Federico II University

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Spontaneous Preterm delivery <34 weeks Less than 34 weeks gestation
Secondary Gestational age Time of delivery
Secondary Birth weight Time of delivery
Secondary Spontaneous preterm birth rates <37, <28 and <24 weeks Less than 24, 28, 34 and 37 weeks gestation
Secondary Spontaneous rupture of membranes Rupture of membranes <34 weeks Less than 34 weeks gestation
Secondary Type of delivery (if cesarean or operativa vaginal or spontaneous vaginal delivery) cesarean delivery, operative vaginal delivery, spontaneous vaginal delivery Time of delivery
Secondary Neonatal death Between birth and 28 days of age
Secondary Composite perinatal outcome Includes necrotizing enterocolitis, intraventricular hemorrhage (grade 3 or higher), respiratory distress syndrome, bronchopulmonary dysplasia (BPD), retinopathy, blood-culture proven sepsis and neonatal death Between birth and 28 days of age
Secondary Maternal side effects Maternal side effects
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