Clinical Trial Details
— Status: Active, not recruiting
Administrative data
NCT number |
NCT02823717 |
Other study ID # |
PERINEE COMPLET |
Secondary ID |
|
Status |
Active, not recruiting |
Phase |
|
First received |
|
Last updated |
|
Start date |
January 31, 2015 |
Est. completion date |
December 31, 2023 |
Study information
Verified date |
April 2023 |
Source |
Groupe Hospitalier Paris Saint Joseph |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational [Patient Registry]
|
Clinical Trial Summary
Perineal tear grade III and IV are relatively common (1-10% of deliveries depending on the
series), and are a source of potentially serious complications, even long time after delivery
(especially disorders of anal continence, psychological trauma). If a number of risk factors
are well described, the support arrangements at the time of delivery and the characteristics
of the review Proctological remote delivery and its relationship to the clinical status of
patients is little known and rarely studied.
In maternity wards of the hospital Saint Joseph Paris and Cochin-Port Royal group, patients
with a diagnosis of severe perineal tear was made are taken following load with common rules,
both for the immediate repair for the remote monitoring. Patients of both sites are indeed
encouraged to consult in proctology consultation in Saint Joseph 4-6 months of birth.
The same support on both sites allows to consider the creation of a relatively homogeneous
cohort in terms of support and consider an important recruitment. Moreover, the geographical
proximity of the inclusions sites (maternity) with proctology service is likely to limit the
risk of lost sight of.
Description:
Main objective / secondary:
Describe exactly the operational management of severe perineal tear (grade III and IV), their
context and the factors associated with them occurring, the results of clinical and
paraclinical proctology examination carried away from the birth, and study their relationship
with the clinical status of patients at 6 months, 1, 2 and 3 years of confinement.
Methodology :
Type prospective, multicentre, non-interventional Study duration: 6 years