Preterm birth (PTB) is associated with over one million infant deaths annually worldwide. The incidence of PTB in the United States is 11.5% with more than 500,000 deliveries occurring at less than 37 weeks gestation annually. The rate of PTB in the United States increased to 12.8% in 2006, and remains high compared to almost all other developed countries, despite the introduction of many public health and medical interventions designed to delay PTB. Weekly treatment with 17-alpha hydroxyprogesterone caproate beginning at 16-20 weeks gestation has been shown to significantly reduce the risk of PTB and is currently recommended for women who experienced spontaneous PTB in a prior pregnancy. However, a strategy for the prevention of spontaneous PTBs in which therapeutic intervention is restricted to women with a previous PTB is likely to have a small effect on the overall rate of prematurity since only about 10% of spontaneous PTBs arise in women with such a history. A major reduction in rates of mortality and morbidity in premature babies will only be achieved with increased precision in the identification of women at risk of spontaneous PTB and through the development of an effective prevention for this complication. Transvaginal ultrasound measurement of cervical length is a reliable screening test for prediction of PTB. Although treatment with vaginal progesterone is effective in decreasing PTB in women with a short cervix, over 30% of women still experience premature delivery and many women find daily administration of progesterone to be challenging. Preliminary studies have suggested that use of an intravaginal pessary may be effective in preventing PTB. If effective this approach would be particularly appealing because of the wide availability of pessaries, ease of use, and low cost. Unfortunately, existing studies are inadequate to confirm effectiveness; a well designed, properly powered, prospective randomized trial is warranted prior to widespread implementation in clinical practice. We propose such a trial to study the effectiveness of the pessary in decreasing the incidence of PTB in an inner city Philadelphia population.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
122
Geisinger Medical Center
Danville, Pennsylvania, United States
Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania, United States
Pennsylvania Hospital
Philadelphia, Pennsylvania, United States
Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, United States
Number of Subjects Experiencing Preterm Birth
Birth before 37 weeks gestation was captured.
Time frame: Before 37 weeks gestation (20 0/7 - 36 6/7 weeks)
Average Birth Weight of Babies Born on Trial
The birth weights of babies born in the pessary group was compared to those born in the no pessary group
Time frame: Time of delivery
Number of Participants That Experienced Spontaneous Preterm Births on Trial
The number of spontaneous births that occurred in participants on trial before 37 weeks was captured.
Time frame: Before 37 weeks gestation
Number of Participants Experiencing Spontaneous Rupture of Membranes
Rupture of membranes before 34 weeks gestation was captured in each group.
Time frame: Less than 34 weeks gestation
Number of Subjects Experiencing Neonatal Death
Number of participants who experienced neonatal deaths from birth to day 28 was captured for each group.
Time frame: Between birth and 28 days of age
Number of Subjects Experiencing Chorioamnionitis
The AE of Chorioamnionitis was captured for each group.
Time frame: Time of delivery
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