RECRUITING

24-Hydroxylase Deficiency and CYP24A1 Mutation Patient Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

You are being asked to take part in this research registry because you or your family member is suspected to have a 24-hydroxylase deficiency.

Official Title

24-Hydroxylase Deficiency and CYP24A1 Mutation Patient Registry

Quick Facts

Study Start:2017-10-19
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03478761

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Urinary Stone Disease
  2. * Nephrocalcinosis
  3. * Metabolic Bone Disease
  4. * Serum Calcium \>/= 9.6 mg/dL
  5. * Parathyroid hormone (PTH) \< 30 pg/mL
  6. * 1,25-dihydroxyvitamin D \> 40 pg/mL OR a family member of a patient who meets the above criteria
  1. * Sarcoidosis
  2. * Lymphoma
  3. * Tuberculosis
  4. * Fungal infections
  5. * Excessive exogenous calcium or vitamin D intake

Contacts and Locations

Study Contact

Barb M Seide, CCRP
CONTACT
507-255-0387
seide.barbara@mayo.edu
Rare Kidney Stone Consortium
CONTACT
800-270-4637
RareKidneyStones@mayo.edu

Principal Investigator

David Sas, MD
PRINCIPAL_INVESTIGATOR
Mayo Clinic
Peter Tebben, MD
STUDY_DIRECTOR
Mayo Clinic

Study Locations (Sites)

Mayo Clinic
Rochester, Minnesota, 55905
United States

Collaborators and Investigators

Sponsor: Mayo Clinic

  • David Sas, MD, PRINCIPAL_INVESTIGATOR, Mayo Clinic
  • Peter Tebben, MD, STUDY_DIRECTOR, Mayo Clinic

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2017-10-19
Study Completion Date2025-12

Study Record Updates

Study Start Date2017-10-19
Study Completion Date2025-12

Terms related to this study

Keywords Provided by Researchers

  • CYP24A1 mutation
  • CYP24A1
  • 24-hydroxylase deficiency

Additional Relevant MeSH Terms

  • 24-hydroxylase Deficiency