Prediction of Recurrence and Complications of Nephrolithiasis Using a Precision Medicine Approach (PRECILITH)

  • STATUS
    Recruiting
  • End date
    Feb 24, 2031
  • participants needed
    2000
  • sponsor
    Centre Hospitalier Universitaire, Amiens
Updated on 24 March 2022

Summary

Nephrolithiasis is a disease caused by the formation of kidney stones in the urinary tract which can then partially or completely obstruct the latter causing an extremely sharp pain called renal colic. In industrialized countries, it affects 10 to 20% of the population, and is the most common kidney disease.The primary objective of this study is to identify the clinical, biological, genetic, molecular and environmental determinants predictive of recurrence of renal lithiasis.

The study follow-up visit schedule corresponds to the visits usually scheduled as part of patient care: 1 year from the inclusion visit (A1), 3 years (A3) then 5 years (A5). Samples for research (additional volume of blood, urine) will be taken by a registered nurse along with the routine check-up samples.Samples intended for research will be sent by staff to the Biobanque de Picardie (CHU Amiens-Picardie) for processing and conservation.

Details
Condition Kidney Stone, Nephrolithiasis
Treatment blood and urine samples
Clinical Study IdentifierNCT05237063
SponsorCentre Hospitalier Universitaire, Amiens
Last Modified on24 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Adults (≥18 years old), male or female
Persons able to understand and object to the information provided (at the discretion of the investigator)
Patient affiliated to social security
Patient agreeing to sign the informed consent form
patient having presented at least one renal colic attack before inclusion

Exclusion Criteria

Pregnant or breastfeeding woman
Persons deprived of liberty
Adults under legal protection guardianship, or curators or unable to express their consent
Patient refusing to participate in the study
Patient in an emergency situation
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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