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Cervical Insufficiency clinical trials

View clinical trials related to Cervical Insufficiency.

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NCT ID: NCT05863481 Completed - Pre-Term Clinical Trials

Obstetric Outcome in Pregnancies Treated With Laparoscopic Cerclage

Start date: May 1, 2011
Phase:
Study type: Observational

Preterm birth is a leading cause of neonatal mortality and morbidity. Cervical insufficiency is one factor implicated in the complex mechanisms involved in spontaneous preterm birth. Trans-abdominal insertion of a cervical cerclage suture can be used to treat cervical insufficiency. Growing evidence support that laparoscopic cerclage procedures are safe and effective. Still, many aspects of the laparoscopic cerclage remains uncertain. Therefore, the investigators plan to study the obstetric outcome from the first and subsequent pregnancies after laparoscopic cerclage in a Danish cohort from Aarhus University Hospital in a 10 years' period.

NCT ID: NCT04722536 Completed - Clinical trials for Cervical Insufficiency

Effectiveness of Cervico-isthmic Cerclage

CERCEI LB
Start date: June 13, 2021
Phase:
Study type: Observational

This study compares the rate of live births before and after cervico-isthmic cerclage in 3 hospitals in the last 10 years. The hypothesis is that cerclage significantly increases the rate of live births in women with cervical insufficiency.

NCT ID: NCT04158401 Completed - Pregnancy Related Clinical Trials

Cervical Stiffness Measurement in Cervical Insufficiency

Start date: January 15, 2020
Phase:
Study type: Observational

The goal of this cross sectional study is to evaluate the differences in cervical stiffness between patients who present for cerclage placement versus normal pregnancies. The central hypothesis is that women for whom a cerclage is indicated will have cervical stiffness measurements lower than normal controls. Cervical stiffness will be objectively measured by the closing pressure Pcl using the Pregnolia measurement device. This is performed during a speculum exam by placing the measurement probe on the ectocervix. In current clinical care, there is no objective measurement of cervical stiffness. An accurate measurement of cervical stiffness that correlates with clinical outcome will advance the field. Successful completion of the current study will spark future studies that correlate cervical stiffness pcl in a prospective study.

NCT ID: NCT02405455 Completed - Clinical trials for Cervical Insufficiency

Cerclage vs Cervical Pessary in Women With Cervical Incompetence

CEPEIC
Start date: June 2015
Phase: N/A
Study type: Interventional

Cervical insufficiency (CI), responsible for 8% of preterm births (PB), is used to describe painless cervical dilation leading to recurrent second-trimester pregnancy losses/births of otherwise normal pregnancies. Structural weakness of cervical tissue was thought to cause or contribute to these adverse outcomes. The term has also been applied to women with one or two such losses/births or at risk for second-trimester pregnancy loss/birth. Cervical pessary and cervical cerclage are both considered as preventive treatments in women at risk for PB. This study aims to demonstrate that the cervical pessary could reduce the preterm birth rate before 37 weeks of gestation in women with prior PB due to cervical insufficiency or in women with prior PB and a short cervix in the current pregnancy.

NCT ID: NCT01114516 Completed - Clinical trials for Cervical Insufficiency

Multifactorial Approach to Emergent Cerclage

RECIA
Start date: March 2010
Phase: N/A
Study type: Interventional

Though cervical insufficiency is a common cause of second trimester pregnancy loss, the placement of an emergent cerclage in these patients is thought to improve perinatal outcomes. It is unknown whether the use of tocolytics and antibiotics prolongs pregnancies complicated by need for emergent cerclage. The objective is to determine whether administration of peri-operative antibiotics and indomethacin to patients receiving emergent cerclages for cervical insufficiency increases latency period to delivery compared with patients receiving emergent cerclage alone.