Physical Examination-Indicated Pessary
Primary Purpose
PreTerm Birth
Status
Withdrawn
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Arabin Pessary
Cervical cerclage
Sponsored by

About this trial
This is an interventional treatment trial for PreTerm Birth
Eligibility Criteria
Inclusion Criteria:
- Singleton pregnancies
- Cervical dilation between 1 to 5 cm and/or visible membranes by pelvic exam or speculum exam between at 16-23 6/7 weeks gestation
Exclusion Criteria:
- Pessary or cerclage already in situ
- active vaginal bleeding
- Placenta previa/accreta
- Multiple gestations
- Amniotic membranes prolapsed beyond external os into the vagina, unable to visualize cervical tissue
- Ruptured amniotic membranes at the time of diagnosis of dilated cervix
- Cervical dilation more than 5 cm
- Labor (progressing cervical dilation) or painful regular uterine contractions
Sites / Locations
- Gabriele Saccone
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Cervical pessary
Cervical cerclage
Arm Description
Arabin Pessary
McDonald Cerclage
Outcomes
Primary Outcome Measures
Neonatal survival
Secondary Outcome Measures
Preterm birth
<24, <28, <30 weeks. both spontaneous and indicated
Latency
Time from randomization to delivery
Birth weight
in grams
gestational age at delivery
mean of delivery
Full Information
NCT ID
NCT02967445
First Posted
November 11, 2016
Last Updated
November 15, 2018
Sponsor
Federico II University
1. Study Identification
Unique Protocol Identification Number
NCT02967445
Brief Title
Physical Examination-Indicated Pessary
Study Type
Interventional
2. Study Status
Record Verification Date
November 2018
Overall Recruitment Status
Withdrawn
Why Stopped
never started
Study Start Date
November 2016 (Actual)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
March 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federico II University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Cervical insufficiency, previously referred to as cervical incompetence, has classically been defined as painless dilation of the cervix in the absence of contractions or bleeding in the second trimester resulting in recurrent pregnancy losses. Painless mid-trimester cervical dilation is an uncommon finding in the general population occurring in less than 1% of pregnancies. Cerclage for the prevention pregnancy loss in cases with both prior preterm births and/or second trimester losses, as well as second trimester cervical dilatation in the index pregnancy, was first reported in the 1950's. Cerclage placement in this setting has been variably referred to as "physical exam-indicated cerclage", "rescue cerclage", and "emergency cerclage". To date, the benefits of cerclage for this indication are not entirely clear.
A recent meta-analysis showed that physical exam-indicated cerclage is associated with a reduction in perinatal mortality and prolongation of pregnancy when compared to no such cerclage.
Recently, several RCTs have shown that cervical pessary could decrease the incidence of PTB in several populations.
Thus, the aim of our trial as noninferiority trial is to evaluate the efficacy of pessary compared to cervical cerclage in prevention of PTB in women in the setting of mid-trimester cervical dilation
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreTerm Birth
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cervical pessary
Arm Type
Experimental
Arm Description
Arabin Pessary
Arm Title
Cervical cerclage
Arm Type
Active Comparator
Arm Description
McDonald Cerclage
Intervention Type
Device
Intervention Name(s)
Arabin Pessary
Intervention Description
Arabin silicon pessary
Intervention Type
Device
Intervention Name(s)
Cervical cerclage
Primary Outcome Measure Information:
Title
Neonatal survival
Time Frame
From delivery to 28 days
Secondary Outcome Measure Information:
Title
Preterm birth
Description
<24, <28, <30 weeks. both spontaneous and indicated
Time Frame
time of delivery
Title
Latency
Description
Time from randomization to delivery
Time Frame
time of delivery
Title
Birth weight
Description
in grams
Time Frame
time of delivery
Title
gestational age at delivery
Description
mean of delivery
Time Frame
time of delivery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Singleton pregnancies
Cervical dilation between 1 to 5 cm and/or visible membranes by pelvic exam or speculum exam between at 16-23 6/7 weeks gestation
Exclusion Criteria:
Pessary or cerclage already in situ
active vaginal bleeding
Placenta previa/accreta
Multiple gestations
Amniotic membranes prolapsed beyond external os into the vagina, unable to visualize cervical tissue
Ruptured amniotic membranes at the time of diagnosis of dilated cervix
Cervical dilation more than 5 cm
Labor (progressing cervical dilation) or painful regular uterine contractions
Facility Information:
Facility Name
Gabriele Saccone
City
Napoli
ZIP/Postal Code
80129
Country
Italy
12. IPD Sharing Statement
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Physical Examination-Indicated Pessary
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