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Evaluation of muLtimodal and Non-invasive SPINa Bifida Neurovessels During Prospective Follow-up (SPINLESS)

R

Rennes University Hospital

Status

Enrolling

Conditions

Spina Bifida

Treatments

Biological: Collection of a urine sample
Diagnostic Test: Magnetic Resonance Imaging of the bladder

Study type

Interventional

Funder types

Other

Identifiers

NCT06041334
35RC20_9746_SPINLESS
IDRCB (Other Identifier)

Details and patient eligibility

About

The aim of the study is to investigate known urinary biomarkers in order to determine whether they can be predictive of a risk of damage to the upper urinary tract and therefore the kidneys in patients with spina bifida. The risk of damage to the upper urinary tract can be calculated using the Galloway score, based on the results of the urodynamic study and retrograde urethrocystography, which all patients with spina bifida have regularly.

The urinary biomarkers studied TIMP-2 (Tissue inhibitor of metalloproteinases 2) and MMP-2 (matrix metalloproteinase-2) are potentially associated with renal degradation, but this has not yet been demonstrated.

Volunteers to take part in the study will have their biomarkers measured at the time of their urodynamic assessment.

Enrollment

50 estimated patients

Sex

All

Ages

6+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Spina patients consulted as part of the multidisciplinary consultation of the spina bifida rare disease reference centre;
  • Written consent to participate in the research.
  • Compulsory membership of a social security scheme

Exclusion criteria

  • Patients with a non-continuous trans ileal urinary diversion ;
  • Patients with enterocystoplasty;
  • Untreated bacteriuria at the time of urodynamic assessment and urine sample collection;
  • History of urinary tract tumour;
  • History of histologically proven interstitial cystitis;
  • Persons under legal protection (safeguard of justice, curatorship, guardianship);
  • Persons deprived of their liberty.
  • Women claiming to be pregnant

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Study volunteers
Other group
Treatment:
Diagnostic Test: Magnetic Resonance Imaging of the bladder
Biological: Collection of a urine sample

Trial contacts and locations

1

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Central trial contact

LOÏC JACOB

Data sourced from clinicaltrials.gov

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