Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06815107

Risk Factors for Poor Tolerance of Ureteral Double-J Stent

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Centre Hospitalier Universitaire, Amiens · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The placement of a Ureteral Double-J Stent as an emergency treatment or preparation for endoscopy after Colic nephritis is very frequent. It is often poorly supported, most often by young patients. A rich symptomatology is related to the probe responsible for a limitation of activities that can have a strong socio-economic impact. The objective of this study is the identification of the predictive factors of poor tolerance.

Conditions

Interventions

TypeNameDescription
OTHERquestionnaryOn day 1 of an ureteral double J stenting, each participant will receive the first USSQ questionnaire, in the French validated version. This questionnaire will be completed at home, one week after the intervention and returned at the following consultation or hospitalization.
OTHERUSSQ surveyif the stent is removed less than 6 months later, the second USSQ survey, in the French validated version will be given to the patient when removing the stent. This questionnaire will be completed at home one week after removal of the stent and return to the referent hospital. If the patient does not return the second questionnaire, our team may contact them by phone to complete it.

Timeline

Start date
2020-04-15
Primary completion
2021-04-15
Completion
2026-04-01
First posted
2025-02-07
Last updated
2025-02-07

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06815107. Inclusion in this directory is not an endorsement.