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Completed
NCT03472066
Measurement of the Cervix During Pregnancy According to Age of Conization
Conditions: Cervix; Pregnancy
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 2
Sponsor: Centre Hospitalier Universitaire, Amiens
Location: CHU Amiens-Picardie Amiens
Summary
Treatment of precancerous lesions of the cervix by conization has been shown to increase the risk of premature delivery and premature rupture of the membranes. It has now been clearly established that the cervix is a growing organ during adolescence and early adulthood, It has been hypothetized that cervical conization during the growth phase reduced its growth potential, and induced shorter cervix during the upcoming pregnancy. No studies have been conducted investigating the age at which conization no longer had an impact on cervical size during pregnancy. This will help to identify the age at conisation below which patients will be identified as being at risk event, and thus offer increased monitoring and possibly prophylactic management by programmed strapping. We propose to measure the length of the cervix of pregnant patients who have benefited from conization, which is currently recommended by the Collège National des Gynécologues Obstetriciens Français .In addition, the investigators will use a control group consisting of non-con conical, parity-matched pregnant patients in whom a cervical measurement will also be performed.
Eligibility Criteria
Inclusion Criteria:
1. Patient referred since January 2008 with pregnancy between 2008 and 2017
2. Pregnancy after conisation
3. Cervix size between 21 and 24 SA before any obstetric event
4. Control group: parity matching, asymptomatic patients
Exclusion Criteria:
1. Threat of late miscarriage,
2. Premature rupture of membranes before cervical echography,
3. Other pregnancies after study of 1st pregnancy after conisation,
4. No measurement of the conization specimen,
5. Lost to follow-up,
6. Age \
Source: ClinicalTrials.gov (NCT03472066). StuddyBuddy aggregates publicly available trial information.