RECRUITING

Vitamin D Homeostasis in Sarcoidosis

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

This study evaluates the relationship between vitamin-D status and severity of sarcoidosis, and the effects of vitamin-D repletion in vitamin-D insufficient patients with sarcoidosis. Half the patients with sarcoidosis who are vitamin-D insufficient will receive standard vitamin-D supplementation via standard regimen while the other half will receive a placebo. Sarcoidosis patients who are vitamin-D sufficient will also act as controls.

Official Title

Vitamin D Homeostasis in Sarcoidosis

Quick Facts

Study Start:2010-07-01
Study Completion:2026-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03621553

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:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Stable medical condition defined as no hospitalization or emergency room visit in the previous 3 months
  2. * No evidence of active pulmonary or systemic infection
  3. * No other active inflammatory disease,
  4. * No active malignancy.
  5. * Normal serum ionized calcium level
  1. * Hospitalization or emergency room visit in the previous 3 months
  2. * Evidence of active pulmonary or systemic infection
  3. * Evidence of active other inflammatory disease
  4. * Evidence of active malignancy
  5. * Elevated serum ionized calcium level

Contacts and Locations

Study Contact

Connie Hsia, MD
CONTACT
2146483426
Connie.Hsia@utsouthwestern.edu
Khashayar Sakhaee, MD
CONTACT
2146480324
Khashayar.Sakhaee@utsouthwestern.edu

Principal Investigator

Connie Hsia, MD
PRINCIPAL_INVESTIGATOR
University of Texas Southwestern Medical Center

Study Locations (Sites)

University of Texas Southwestern Medical Center, and Parkland Health and Hospital System
Dallas, Texas, 75390-9034
United States

Collaborators and Investigators

Sponsor: University of Texas Southwestern Medical Center

  • Connie Hsia, MD, PRINCIPAL_INVESTIGATOR, University of Texas Southwestern Medical Center

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 Date2010-07-01
Study Completion Date2026-12-30

Study Record Updates

Study Start Date2010-07-01
Study Completion Date2026-12-30

Terms related to this study

Additional Relevant MeSH Terms

  • Sarcoidosis
  • Vitamin D Insufficiency