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Clinical Trials/NCT03472066
NCT03472066CompletedNot Applicable

Measurement of the Cervix During Pregnancy According to Age of Conization

Centre Hospitalier Universitaire, Amiens1 site in 1 country2 target enrollmentStarted: October 4, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
2
Locations
1
Primary Endpoint
The main objective is to study the correlation between the size of the cervix and the age at conization. age at conization

Study Overview

Brief 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.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient referred since January 2008 with pregnancy between 2008 and 2017
  • •Pregnancy after conisation
  • •Cervix size between 21 and 24 SA before any obstetric event
  • •Control group: parity matching, asymptomatic patients

Exclusion Criteria

  • •Threat of late miscarriage,
  • •Premature rupture of membranes before cervical echography,
  • •Other pregnancies after study of 1st pregnancy after conisation,
  • •No measurement of the conization specimen,
  • •Lost to follow-up,
  • •Twin Pregnancies
  • •Patient under guardianship

Arms & Interventions

a group of women who have been conized

Previous conization

Intervention: Previous conization (Other)

control group with asymptomatic patients

on routine second trim no previous conization

Intervention: no previous conization (Other)

Outcomes

Primary Outcomes

The main objective is to study the correlation between the size of the cervix and the age at conization. age at conization

Time Frame: 1 day

Cervix length Measured during the second semester echography

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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