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RecruitingNCT02887781TSARUpdated Jan 5, 2024

Clinical Presentation and Renal Outcome of Patients With Tuberous Sclerosis Complex and/or Renal Angiomyolipoma in the Great West Region of France

An observational study in Tuberous Sclerosis Complex, sponsored by University Hospital, Brest. Recruiting at 2 sites in France. Open to participants aged 8 Years and older. Per ClinicalTrials.gov, last updated 2024-01-05.

Sponsored by University Hospital, Brest · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as recruiting.
  • Started Aug 2015; still recruiting 11 years 2 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
8 Years and older
Sex
All
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Study summary

This study aims to investigate the factors (clinical, care-related and genetic) affecting renal outcome in patients with TSC (Tuberous sclerosis complex)

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Conditions studied

  • Tuberous Sclerosis Complex

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In context

Tuberous Sclerosis

115 studies on the registry are indexed under Tuberous Sclerosis; 27 are open to participants now.

This study's planned enrollment of 150 is close to the median of 150 across 37 observational studies indexed under Tuberous Sclerosis.

Browse Tuberous Sclerosis studies →

Lead sponsor

University Hospital, Brest is the lead sponsor of 601 studies on the registry; 136 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
8 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with TSC and followed in one of the nephrology centers in the West of France

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient presenting with an isolated angiomyolipoma or
  • Patient presenting with tuberous sclerosis complex combined with an angiomyolipoma or
  • Patient presenting with tuberous sclerosis complex
  • Patient not objecting to the study

Exclusion criteria

Exclusion criteria of study participants

■Patient objecting to the study

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
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What researchers measure

Primary outcomes

  1. Evolution of the renal function estimated by the MDRD GFR

    Time frame: 18 months after inclusion

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Study locations

2 of 2 sites recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02887781
Responsible party
Sponsor
First posted
Sep 2, 2016
Start date
Aug 13, 2015
Primary completion
Dec 31, 2024 (estimated)
Completion
Dec 31, 2024 (estimated)
Last update
Jan 5, 2024

Study contacts

Yannick LE MEUR, MD PhD
Contact
yannick.lemeur@chu-brest.fr
Yannick LE MEUR, MD PhD
study director · University Hospital, Brest
View the source record on ClinicalTrials.gov ↗

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