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
| Type | Name | Description |
|---|---|---|
| OTHER | questionnary | On 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. |
| OTHER | USSQ survey | if 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.