Rare Kidney Stone Consortium Biobank

Conditions

• APRT Deficiency
• Cystinuria
• Dent Disease
• Primary Hyperoxaluria

Eligibility Criteria

Sex

ALL

Age

N/A - N/A

Healthy Volunteers

Not accepted

Study Details

This study is being done to obtain samples from patients with primary hyperoxaluria, cystinuria, adenine phosphoribosyl transferase (APRT) deficiency, and Dent disease, and from their family members, for use in future research.

Key Dates

Start date

May 31, 2013

Status verified

Jul 2025

Primary completion

Jun 30, 2030

Completion

Jun 30, 2030

Study Design

Enrollment

2,000 participants (estimated)

Arms

• Arm: Primary Hyperoxaluria
  Diagnosis of Primary Hyperoxaluria, or a family member of someone with this diagnosis.
• Arm: Dent Disease
  Diagnosis of Dent Disease, or a family member of someone with this diagnosis.
• Arm: Cystinuria
  Diagnosis of Cystinuria, or a family member of someone with this diagnosis.
• Arm: APRT deficiency
  Diagnosis of APRT Deficiency, or a family member of someone with this diagnosis.

Primary Outcome Measure

Number of samples stored in tissue bank [ Time Frame: 4 years ]

Central Contacts

• Barb M Seide
  507-255-0387
  [email protected]
• Leah M Knoke
  507-293-0467
  [email protected]

Locations (1)

Find similar trials in Rochester, MN

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