Clinical Trials Directory

Trials / Unknown

UnknownNCT02823717

Obstetric and Proctology Support of Patients With Perineums Suits

Obstetric and Proctology Support of Patients With Perineums Suits. Prospective Cohort

Status
Unknown
Phase
Study type
Observational
Enrollment
186 (actual)
Sponsor
Fondation Hôpital Saint-Joseph · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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

Conditions

Timeline

Start date
2015-01-31
Primary completion
2018-01-31
Completion
2023-12-31
First posted
2016-07-06
Last updated
2023-04-27

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02823717. Inclusion in this directory is not an endorsement.