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Cervical Occlusion Double-level Stitch Application

Not Applicable
Recruiting
Conditions
Cervical Incompetence
Interventions
Procedure: Double-level cervical cerclage
Procedure: Single-level cervical cerclage
Registration Number
NCT05268640
Lead Sponsor
Centre of Postgraduate Medical Education
Brief Summary

Cervical insufficiency is defined as painless dilatation of the cervix during the second trimester of pregnancy. As a result of shortening and opening of the cervix, despite the lack of uterine contractions, the fetal membranes invade into the cervical canal and then into the vagina, which results in premature rupture of the membranes and miscarriage or preterm delivery. Cervical insufficiency occurs in approximately 1% of the women. The aim of the study is to evaluate the effectiveness of placing a double-level cervical cerclage in the treatment of advanced cervical insufficiency. The hypothesis assumes that the insertion of a double-level suture is associated with a reduction in the rate of deliveries \< 34 weeks of gestation in comparison to single-level suture. The study will include women with fetal membranes visible through open external os of the cervix between 16+0 and 23+6 weeks. They will be randomized to two arms - McDonald's single cervical cerclage or two-level cerclage.

Detailed Description

This is an open-label, multicentre, prospective, randomised controlled trial (RCT). Women will be randomized to the single-level cerclage arm or the double-level cerclage. Each patient will have a vaginal swab for aerobic and anaerobic bacteria and fungi culture, as well as for mycoplasmas, chlamydia and ureaplasma performed. Each patient will be treated with progesterone (vaginally 2 x 100 mg per day) and empirical antibiotic therapy (ceftriaxone 2.0 g iv + clarithromycin 2 x 500 mg po + metronidazole 3 x 500 mg iv for 7 days). If specific pathogens will be detected, the antibiotic therapy will be modified according to the antibiogram. If the diagnosis of cervical insufficiency will be made \>23 weeks of gestation a single course of corticosteroid therapy will be administered (betamethasone 2 x 12 mg im) if the rsik of delivery within 7 days will be assessed as high. Indomethacin will also be administered for 48 hours (starting the day of cerclage administration, indomethacin 2 x 75 mg po for 48 hours). In the single-level cerclage arm McDonald suture will be administered. In the double-level cerclage arm two separate sutures analogous to McDonald technique will be placed, one approximately 1 cm higher above the other. Patients will be followed up until miscarriage or delivery and will receive standard perinatal care. Gestational age at delivery, the occurrence of cerclage complications and neonatal outcomes will be analyzed.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
78
Inclusion Criteria
  • singleton pregnancy,
  • gestational age 16+0 to 23+6 weeks,
  • live fetus,
  • cervical incompetence with fetal membranes visible through external os before 24+0 weeks of gestation,
  • informed written consent.

Exclusion Criteria - any of the following occuring before the administration of the cerclage:

  • preterm premature rupture of membranes,
  • vaginal bleeding,
  • active regular uterine contractions,
  • fetal demise,
  • fever,
  • intrauterine infection (diagnosed in case of maternal body temperature ≥ 38°C with no alternative cause identified and at least 2 symptoms among the following appear: fetal tachycardia > 160 bpm for 10 minutes or longer, uterine pain, purulent vaginal discharge, white blood cell count > 15 G/L in the absence of corticosteroid treatment or increased plasma C-reactive protein > 10 mg/L),
  • known genetic defects of the fetus,
  • known lethal fetal malformations,
  • congenital uterine defects,
  • multiple pregnancy.
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Double-level cerclageDouble-level cervical cerclagedouble-level cervical cerclage placement with one suture above the other approximately 1 cm higher. Suture will be placed analogous to McDonald technique
Single-level cerclageSingle-level cervical cerclagesingle-level cervical cerclage of McDonald technique
Primary Outcome Measures
NameTimeMethod
deliveries below 34+0 weeks of gestationobservation after intervention for 26 weeks of until birth

number and rate of deliveries below 34+0 weeks of gestation

Secondary Outcome Measures
NameTimeMethod
gestational age at deliveryobservation after intervention for 26 weeks of until birth

duration of pregnancy untill delivery in weeks and days

time from cerclage administration to deliveryobservation after intervention for 26 weeks of until birth

time from cerclage administration to delivery in days

maternal outcomesobservation after intervention for 26 weeks of until birth

maternal mortality, miscarriage, intrauterine infection, prelabour rupture of membranes, o cervical laceration

fetal demiseobservation after intervention for 26 weeks of until birth

number and rate of pregnancies complicated by fetal demise

neonatal outcomesobservation after intervention for 26 weeks of until birth

number and rate of: congenital infections, respiratory morbidity, hospitalizations in the Neonatal Intensive Care Unit, early neurodevelopmental morbidity, gastrointestinal morbidity, retinopathy of prematurity, newborn's death before the discharge home

birth weightobservation after intervention for 26 weeks of until birth

neonatal weight at delivery in grams

5th minute Apgar scoreobservation after intervention for 26 weeks of until birth

neonatal general condition at 5th minute after delivery according to the Apgar Scale

Trial Locations

Locations (7)

1st Department of Obstetrics and Gynecology, Center of Postagraduate Medical Education

🇵🇱

Warsaw, Mazowieckie, Poland

Department of Obstetrics, Women's Diseases and Oncological Gynecology, Nicolaus Copernicus University

🇵🇱

Bydgoszcz, Kujawsko-pomorskie, Poland

Department of Obstetrics, Perinatology and Neonatology, Center of Postagraduate Medical Education

🇵🇱

Warsaw, Mazowieckie, Poland

1st Department of Obstetrics and Gynecology, Medical University of Warsaw

🇵🇱

Warsaw, Mazowieckie, Poland

Department of Obstetrics and Gynecology, Oncological Gynecology and Gynecological Endocrinology, Medical University of Gdansk

🇵🇱

Gdańsk, Pomorskie, Poland

Pomeranian Medical University Szczecin

🇵🇱

Szczecin, Zachodniopomorskie, Poland

Polish Mother's Memorial Hospital - Research Institute

🇵🇱

Łódź, Łodzkie, Poland

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