A Randomized Trial of Pessary in Singleton Pregnancies With a Short Cervix

Preterm Delivery Clinical Trial

— TOPS  

Official title:

A Randomized Trial of Pessary in Singleton Pregnancies With a Short Cervix

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02901626
• Other study ID #: HD36801 - TOPS
• Secondary ID: UG1HD087230UG1HD
• Status: Terminated
• Phase: Phase 3
• Start date: February 14, 2017
• Est. completion date: May 10, 2022

Study information

• Verified date: June 2023
• Source: The George Washington University Biostatistics Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to determine whether the Arabin pessary is a useful intervention of preterm birth at less than 37 weeks in women with a singleton gestation and a short cervix.

Description:

While cervical length is one of the most powerful predictors of subsequent preterm birth, the best treatment to reduce subsequent preterm birth remains unknown. This study is a randomized trial of women who have a singleton pregnancy and a short cervical length on transvaginal ultrasound as determined by a study-certified sonographer. It is being conducted at 12 clinical centers across the country and the recruitment target is enrollment of 850 pregnant women. Participants will be randomized to 1) Arabin pessary or 2) usual care as per by local hospital protocol. Pessary is a promising low-cost, non-surgical intervention that appears to be well-tolerated. The pessary will be placed by obstetric providers trained in appropriate placement of the Arabin pessary. The primary outcome of the study is delivery or fetal death prior to 37 weeks 0 days gestational age.

In the literature, there are two large trials that have produced conflicting results (M Goya et al, 2012, K Nicolaides et al, 2016). Thus, the results of an adequately powered and appropriately conducted trial from the United States will be important in determining whether pessary is a useful intervention for the prevention of subsequent preterm birth in women with singleton gestation.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 544
• Est. completion date: May 10, 2022
• Est. primary completion date: April 2, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Singleton gestation. Twin gestation reduced to singleton either spontaneously or therapeutically, is not eligible unless the reduction occurred before 13 weeks 6 days project gestational age. Higher order multifetal gestations reduced to singletons are not eligible.

• Gestational age at randomization between 16 weeks 0 days and 23 weeks 6 days based on clinical information and evaluation of the earliest ultrasound.

• Cervical length on transvaginal examination of less than or equal to 20 mm by a study certified sonographer. There is no lower cervical length threshold.

Exclusion Criteria:

• Cervical dilation (internal os) 3 cm or greater on digital examination or evidence of prolapsed membranes beyond the external cervical os either at the time of the qualifying cervical ultrasound examination or at a cervical exam immediately before randomization.

• Fetal anomaly or imminent fetal demise. This includes lethal anomalies, or anomalies that may lead to early delivery or increased risk of neonatal death e.g., gastroschisis, spina bifida, serious karyotypic abnormalities. An ultrasound examination from 14 weeks 0 days to 23 weeks 6 days by project Estimated Date of Confinement (EDC) must be performed prior to randomization to evaluate the fetus for anomalies.

• Previous spontaneous preterm birth between 16 weeks 0 days and 36 weeks 6 days. This includes induction for pPROM in a prior pregnancy.

• Planned treatment with intramuscular 17-a hydroxy-progesterone caproate.

• Placenta previa, because of risk of bleeding and high potential for indicated preterm birth. A low lying placenta is acceptable.

• Active vaginal bleeding greater than spotting at the time of randomization, because of potential exacerbation due to pessary placement.

• Symptomatic, untreated vaginal or cervical infection because of potential exacerbation due to pessary placement. Patients may be treated and if subsequently asymptomatic, randomized. However, if it is more than 10 days since the cervical length measurement, a new cervical length measurement must be obtained.

• Active, unhealed herpetic lesion on labia minora, vagina, or cervix due to the potential for significant patient discomfort or increasing genital tract viral spread. Once lesion(s) heal and the patient is asymptomatic, she may be randomized. History of herpes is not an exclusion.

• Rupture of membranes due to likelihood of pregnancy loss and preterm delivery as well as the risk of ascending infection which could be increased with pessary placement.

• More than six contractions per hour reported or documented prior to randomization. It is not necessary to place the patient on a tocodynamometer.

• Known major Mullerian anomaly of the uterus (specifically bicornuate, unicornuate, or uterine septum not resected) due to increased risk of preterm delivery which is unlikely to be affected by progesterone.

• Any fetal/maternal condition which would require invasive in-utero assessment or treatment, for example significant red cell antigen sensitization or neonatal alloimmune thrombocytopenia.

• Major maternal medical illness associated with increased risk for adverse pregnancy outcome or indicated preterm birth (treated hypertension requiring more than one agent, treatment for diabetes prior to pregnancy, chronic renal insufficiency defined by creatinine >1.4 mg/dL, carcinoma of the breast, conditions treated with chronic oral glucocorticoid therapy). Lupus, uncontrolled thyroid disease, and New York Heart Association(NYHA) stage II or greater cardiac disease are also excluded. Patients with seizure disorders, HIV, and other medical conditions not specifically associated with an increased risk of indicated preterm birth are not excluded. Prior cervical cone/LOOP/Loop Electrocautery Excision Procedure (LEEP) is not an exclusion criterion.

• Planned cerclage or cerclage already in place since it would preclude placement of a pessary.

• Planned indicated delivery prior to 37 weeks.

• Allergy to silicone.

• Participation in another interventional study that influences gestational age at delivery or neonatal morbidity or mortality.

• Participation in this trial in a previous pregnancy. Patients who were screened in a previous pregnancy, but not randomized, may be included.

• Prenatal care or delivery planned elsewhere unless the study visits can be made as scheduled and complete outcome information can be obtained.

Related Conditions & MeSH terms

• Premature Birth
• Preterm Delivery
• Short Cervix

Intervention

Device:
• Arabin Cervical Pessary
The Arabin cervical pessary is a soft, flexible silicone pessary and fits high around the cervix with no rigid metal framework or inflexible edges that put increase pressure on the vaginal wall. It is available in a variety of sizes however three sizes will be used in this study: Pessary Size upper diameter, lower diameter Nulliparous 65 mm, 32 mm Multiparous 70 mm, 32 mm Alternative 70 mm, 35 mm

Locations

Country	Name	City	State
United States	University of Alabama - Birmingham	Birmingham	Alabama
United States	University of North Carolina - Chapel Hill	Chapel Hill	North Carolina
United States	Northwestern University	Chicago	Illinois
United States	Case Western Reserve University	Cleveland	Ohio
United States	Ohio State University	Columbus	Ohio
United States	University of Texas Medical Branch	Galveston	Texas
United States	University of Texas - Houston	Houston	Texas
United States	Columbia University	New York	New York
United States	University of Pennsylvania	Philadelphia	Pennsylvania
United States	Magee Womens	Pittsburgh	Pennsylvania
United States	Brown University	Providence	Rhode Island
United States	University of Utah	Salt Lake City	Utah

Sponsors (2)

Lead Sponsor	Collaborator
The George Washington University Biostatistics Center	Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Country where clinical trial is conducted

United States, 

References & Publications (32)

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* Note: There are 32 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Preterm Delivery or Fetal Death at Less Than 37 Weeks.	Participants who either delivered or experienced a fetal death prior to 37 weeks gestation.	Before 37 weeks 0 days gestation, a period of up to 21 weeks from enrollment.
Secondary	Interval From Randomization to Delivery or Fetal Death	The median interval between randomization to delivery or death of the fetus.	from randomization to delivery or fetal death (up to a length of 189 days)
Secondary	Gestational Age at Delivery	Median gestational age (in weeks) at the time of delivery	From randomization to delivery (up to a length of 189 days)
Secondary	Number of Participants With Preterm Delivery or Fetal Death at Less Than 28 Weeks Gestation	The number of participants who either delivered or experienced a fetal death prior to 28 weeks gestation.	from randomization to less than 28 weeks gestation (a period of less than 91 days)
Secondary	Number of Participants With Preterm Delivery or Fetal Death at Less Than 32 Weeks Gestation	The number of participants who either delivered or experienced a fetal death prior to 32 weeks gestation.	from randomization to less than 32 weeks gestation (a period of less than 119 days)
Secondary	Number of Participants With Preterm Delivery or Fetal Death at Less Than 35 Weeks Gestation	The number of participants who either delivered or experienced a fetal death prior to 35 weeks gestation.	from randomization to less than 35 weeks gestation (a period of less than 140 days)
Secondary	Number of Participants With Preterm Premature Rupture of Membranes	Participants were categorized as yes if the amniotic membranes ruptured prior to labor onset and before 37 weeks gestation.	Before 37 weeks 0 days gestation, a period of up to 21 weeks from enrollment
Secondary	Number of Participants With Spontaneous Preterm Delivery.	The number of participants who experienced spontaneous onset of labor and had an unassisted vaginal delivery prior to 37 weeks gestation. Induction for delivery was not performed and operative techniques such as forceps or vacuum were not used.	From randomization to delivery (up to a length of 189 days)
Secondary	Number of Participants With Indicated Preterm Delivery	The number of participants who underwent labor induction or had an assisted vaginal delivery with forceps or vacuum or cesarean delivery prior to 37 weeks gestation.	from randomization to delivery (up to a length of 189 days)
Secondary	Number of Participants With Cesarean Delivery	The number of participants who underwent a surgical procedure for delivery (cesarean) at any gestational age.	From randomization to delivery (up to a length of 189 days)
Secondary	Number of Participants With Chorioamnionitis	The number of participants who had a clinical diagnosis of chorioamnionitis and a body temperature of at least 100.0° F (38° C) and no other defined infection.	From randomization to delivery (up to a length of 189 days)
Secondary	Median Length of Maternal Antepartum Hospital Stay Before Delivery	Median number of days from maternal hospital admission for delivery and the date of delivery.	from date of admission for delivery up to delivery date (up to 5 days)
Secondary	Number of Participants With Vaginal Infection	The number of participants with a clinical diagnosis of a vaginal infection. Includes participants with at least one study visit.	From randomization to delivery (up to a length of 189 days)
Secondary	The Number of Participants Who Had a Vaginal Infection and Received Antibiotic Treatment, Among All Persons Enrolled With at Least One Study Visit	The number of participants who received antibiotics or antifungal medication for a vaginal infection (out of the total sample for which data is available)	From randomization to delivery (up to a length of 189 days)
Secondary	Number of Participants Treated for Preterm Labor Including Placement of Cerclage	The number of participants who received any one of the following treatments for preterm labor: tocolysis, cerclage, bedrest, antenatal corticosteroids for fetal lung maturity, or magnesium sulfate for neuroprotection.	From randomization to delivery (up to a length of 189 days)
Secondary	Median Duration of Neonatal Ventilator or Continuous Positive Airway Pressure Use	Median number of days a neonate or infant was on a ventilator or received continuous positive airway pressure.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates Requiring Ventilator or Continuous Positive Airway Pressure Use	The number of neonates or infants who required ventilator support or received continuous positive airway pressure.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Median Duration (in Days) of Neonatal Supplemental Oxygen Use	Median number of days a neonate received supplemental oxygen after admission to the NICU or intermediate nursery. Supplemental oxygen is defined as FiO2 > 0.21.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Seizures Requiring Treatment	The number of neonates with a clinical diagnosis of seizures who received anti-seizure medication.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates Small for Gestational Age < 5th Percentile	The number of neonates whose birthweight compared with gestational age at delivery was less than the 5th percentile, as assessed by sex and race, using United States birth certificate data.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Intraventricular Hemorrhage (IVH) Grades III or IV	IVH grades III or IV are as determined by cranial ultrasounds performed as part of routine clinical care and classified based on the Papile classification system	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Retinopathy of Prematurity (ROP)	The number of neonates with a clinical diagnosis of retinopathy of prematurity where an ophthalmologic examination of the retina was performed.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates Experiencing Respiratory Distress Syndrome (RDS)	The number of neonates with a diagnosis of respiratory distress syndrome defined as the presence of clinical signs of respiratory distress (tachypnea, retractions, flaring, grunting, or cyanosis), with oxygen requirement and a chest x-ray that show hypoaeration and reticulogranular infiltrates.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Bronchopulmonary Dysplasia (BPD)	The number of neonates with a clinical diagnosis of bronchopulmonary dysplasia defined as oxygen requirement at 28 days of life if delivered at or after 32 weeks gestation, or at 36 weeks project gestational age if delivered before 32 weeks gestation.	Delivery through 28 days of life if delivered at or after 32 weeks. Delivery through 36 weeks gestation if delivered before 32 weeks.
Secondary	Number of Neonates With Necrotizing Enterocolitis (NEC) Stage 2 or 3	The number of neonates diagnosed with NEC, defined as modified Bell Stage 2 or 3 where stage 2 represents clinical signs and symptoms with pneumatosis intestinalis on radiographs and stage 3 is defined as advanced clinical signs and symptoms, pneumatosis, impending or proven intestinal perforation.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Hyperbilirubinemia	The number of neonates diagnosed with hyperbilirubinemia, defined as peak total bilirubin of at least 15 mg% or the use of phototherapy	delivery through hospital discharge (up to a length of 435 days)
Secondary	Neonatal Infectious Morbidity Including Sepsis, Suspected Sepsis and Pneumonia	The number of neonates diagnosed with any one of the following: Sepsis (within 72 hours and > 72 hours after birth) defined as a clinically ill infant in whom systemic infection is suspected with a positive blood, CSF, or catheterized/suprapubic urine culture; or, in the absence of positive cultures, clinical evidence of cardiovascular collapse or an unequivocal radiograph confirming infection.; Suspected sepsis. The diagnosis of suspected sepsis will include infants with suspicious clinical findings of infection, but no positive cultures or radiographs.; Pneumonia. The diagnosis of pneumonia will be confirmed by radiograph or positive blood culture.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Early Onset Sepsis	The number of neonates with a clinical diagnosis of sepsis within 72 hours of life, defined as a clinically ill infant in whom systemic infection is suspected with a positive blood, cerebrospinal fluid, or catheterized/suprapubic urine culture; or, in the absence of positive cultures, clinical evidence of cardiovascular collapse or an unequivocal radiograph confirming infection.	within 72 hours of birth
Secondary	Number of Neonates With Late Onset Sepsis	The number of neonates with a clinical diagnosis of sepsis at or after 72 hours of life, defined as the presence of a clinically ill infant in whom systemic infection is suspected with a positive blood, cerebrospinal fluid, or catheterized/suprapubic urine culture; or, in the absence of positive cultures, clinical evidence of cardiovascular collapse or an unequivocal radiograph confirming infection.	72 hours of birth or later (up to hospital discharge - a maximum of 435 days)
Secondary	Number of Neonates With Suspected Sepsis	The number of neonates with suspicious clinical findings of infection, but no positive cultures or radiographs.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Pneumonia	The number of neonates with a clinical diagnosis of pneumonia within 72 hours of birth and confirmed by either an x-ray demonstrating consolidation with air bronchograms, or a positive blood culture performed at the time of clinical diagnosis.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Number of Neonates With Composite Outcome	The number of neonates diagnosed with any one of fetal or neonatal death or Respiratory Distress Syndrome, Grade 3 or 4 Intraventricular Hemorrhage, Periventricular Leukomalacia, Stage 2 or 3 Nectrotizing Enterocolitis, Bronchopulmonary Dysplasia, Stage III or higher Retinopathy of Prematurity, or early onset sepsis.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Median Length of Neonatal Hospital Stay	Median number of days the neonate/infant remained in hospital.	delivery through hospital discharge (up to a length of 435 days)
Secondary	Median Number of Days in Neonatal Intensive Care Unit (NICU)	Median number of days the neonate/infant remained in the neonatal intensive care unit or special care nursery.	delivery through hospital discharge (up to a length of 435 days)