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Urinary Calculi After Bladder Augmentation in Children

NCT ID: NCT06734403

Last Updated: 2024-12-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

34 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-11-20

Study Completion Date

2023-04-10

Brief Summary

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The goal of this observational study is to analyse the occurence of urinary calculi after bladder augmentation in children:

* location of the calculi (kidney or bladder)
* type of bladder augmentation with higher rate of urinary calculi and why
* Find risk factors of urinary calculi in bladder augmentation (age, sex, other bladder procedures..)

Detailed Description

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Study the data of patients younger than 18 years old, who underwent a bladder augmentation, complicated by urinary calculi.

Conditions

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Calculi, Urinary Neurogenic Bladder Disorder Spina Bifida Child, Only

Keywords

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Urinary Calculus Bladder Augmentation Child Retrospective Study

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Ileocystoplasty

Urinary Calculi After Ileocystoplasty in Children

Bladder Augmentation

Intervention Type OTHER

Bladder Augmentation using bowel loop (ileal or sigmoid loop)

Sigmoidocystoplasty

Urinary Calculi After Sigmoidocystoplasty in Children

Bladder Augmentation

Intervention Type OTHER

Bladder Augmentation using bowel loop (ileal or sigmoid loop)

Interventions

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Bladder Augmentation

Bladder Augmentation using bowel loop (ileal or sigmoid loop)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients younger than 18 years old, with urinary calculi, after bladder augmentation

Exclusion Criteria

* Patients older than 18 years old, with urinary calculi, after bladder augmentation
Minimum Eligible Age

0 Years

Maximum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role collaborator

University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Destinval Christelle

M.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University Hospital, Clermont-Ferrand

Clermont-Ferrand, Auvergne, France

Site Status

Countries

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France

Other Identifiers

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M24DC1104

Identifier Type: -

Identifier Source: org_study_id

NCT05861024

Identifier Type: -

Identifier Source: nct_alias