Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Constipation
  • Peritoneal Dialysis Complication
Type
Observational
Design
Observational Model: OtherTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Patients included in this trial will be monitored as part of the usual management of their pathology, a Terminal Chronic Kidney Disease treated by the Peritoneal Dialysis technique. During this treatment, patients will be follow every 2 months in consultation in the Metabolic Diseases Department of ...

Patients included in this trial will be monitored as part of the usual management of their pathology, a Terminal Chronic Kidney Disease treated by the Peritoneal Dialysis technique. During this treatment, patients will be follow every 2 months in consultation in the Metabolic Diseases Department of the Hospital of Vichy. These consultations include: Pre-selection consultation/Inclusion (visit to J0 -3 months) Half-yearly review (visit J0, visit at 12 months and visit at 24 months) Simple consultation (visits to 2, 4, 8, 10, 14, 16, 20, 22 months) Annual review (visits at 6 and 18 months) In this prospective trial, there is no intervention on the patient; They will only have to complete questionnaires on their intestinal transit (Charlson Scale, Katz Scale, Neurological Functional Score, Intestinal Function Index, Severity Score for constipation, Bristol Scale, Constipation Assessment Scale, Constipation Risk Assessment Scale). No minimal risk and constraint is identified, excluding our trial from the category of interventional research. The category 3 (non-interventional trial) of the jardé classification is therefore accepted.

Tracking Information

NCT #
NCT04102527
Collaborators
University Hospital, Clermont-Ferrand
Investigators
Not Provided