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Vitamin D Homeostasis in Sarcoidosis

Primary Purpose

Sarcoidosis, Vitamin D Insufficiency

Status
Active
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ergocalciferol
Placebo
Calcium Citrate with Vitamin D2
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sarcoidosis

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Stable medical condition defined as no hospitalization or emergency room visit in the previous 3 months
  • No evidence of active pulmonary or systemic infection
  • No other active inflammatory disease,
  • No active malignancy.
  • Normal serum ionized calcium level

Exclusion Criteria:

  • Hospitalization or emergency room visit in the previous 3 months
  • Evidence of active pulmonary or systemic infection
  • Evidence of active other inflammatory disease
  • Evidence of active malignancy
  • Elevated serum ionized calcium level

Sites / Locations

  • University of Texas Southwestern Medical Center, and Parkland Health and Hospital System

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

Other

Arm Label

Low vit-D, Ergocalciferol

Low vit-D, Placebo

Normal vit-D, control

Arm Description

Low serum vitamin D level, split by use or non-use of systemic corticosteroid. Vitamin D2 (Ergocalciferol) 50,000 units will be given by mouth once a week for 12 weeks, then once a month for 12 weeks. Daily dietary requirement (calcium citrate with vitamin D2 (200 mg/250 Units tablets, 4 tablets per day) will be given by mouth for 24 weeks).

Low serum vitamin D level, split by use or non-use of systemic corticosteroid. Placebo capsules of identical size and appearance will be given by mouth once a week for 12 weeks, then once a month for 12 weeks. Daily dietary requirement (calcium citrate with vitamin D2 (200 mg/250 Units tablets, 4 tablets per day) will be given by mouth for 24 weeks).

Normal serum vitamin D level, split by use or non-use of systemic corticosteroid. Daily dietary requirement (calcium citrate with vitamin D2 (200 mg/250 Units tablets, 4 tablets per day) will be given by mouth for 24 weeks).

Outcomes

Primary Outcome Measures

Change in lung function from baseline
(Measurement at end of study)/(measurement at enrollment)

Secondary Outcome Measures

Change in King's Sarcoidosis Questionnaire Score
Standard validated questionnaire for assessing the impact of sarcoidosis on quality of life. Questions address symptoms, activities and psychosocial impacts of disease. It consists of 29 questions on general health, medications, and symptoms in lung, skin, and eyes, summed to derive a total score. Each question is scored on a scale of 1 (worst) to 7 (best). Minimum total score = 5 (poorest health). Maximum total score = 203 (best health).
Change in six minute walk distance
(Measurement at end of study)/(measurement at enrollment)
Change in blood cell counts from complete blood count (CBC)
(Measurement at study point)/(initial measurement at enrollment)
Change in metabolic profile from complete metabolic panel (CMP)
(Measurement at study point)/(initial measurement at enrollment)
Change in serum vitamin-D metabolite concentration
(Measurement at study point)/(initial measurement at enrollment)
Change in serum angiotensin converting enzyme (ACE) concentration
(Measurement at study point)/(initial measurement at enrollment)
Change in serum serum gamma-globulin concentration
(Measurement at study point)/(initial measurement at enrollment)
Change in serum C-reactive protein (CRP) concentration
(Measurement at study point)/(initial measurement at enrollment)
Change in serum tumor Necrosis factor-alpha (TNF-alpha) concentration
(Measurement at study point)/(initial measurement at enrollment)
Change in serum interferon-gamma (IFN-gamma) concentration
(Measurement at study point)/(initial measurement at enrollment)
Changes in serum interleukin concentration
(Measurement at study point)/(initial measurement at enrollment)
Change in 24 hour urine calcium/creatinine ratio
(Measurement at study point)/(initial measurement at enrollment)
Change in 24 hour urine deoxypyridinoline concentration
(Measurement at study point)/(initial measurement at enrollment)
Change in fractional lung tissue volume on computed/positron emission tomography (PET/CT)
(Measurement at end of study)/(measurement at enrollment)
Change in Fluoro-deoxyglucose (FDG) uptake on PET/CT
(Measurement at end of study)/(measurement at enrollment
Change in bone density z-score
(Measurement at end of study)/(measurement at enrollment)

Full Information

First Posted
July 17, 2018
Last Updated
June 6, 2023
Sponsor
University of Texas Southwestern Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03621553
Brief Title
Vitamin D Homeostasis in Sarcoidosis
Official Title
Vitamin D Homeostasis in Sarcoidosis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 1, 2010 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
Sarcoidosis is a multi-system inflammatory disease characterized by T-helper lymphocyte hyperactivity leading to granulomatous inflammation. The granuloma cells autonomously convert 25-hydroxy-vitamin-D (25OHD) to the active metabolite 1,25-dihydroxy-vitamin-D (1,25OH2D) independent of normal feedback control but dependent on substrate (25OHD) concentration. Circulating 1,25OH2D exerts both anti-inflammatory and mineral metabolic actions. Deficiency of 25OHD limits substrate-dependent 1,25OH2D synthesis, diminishes anti-antigenic innate immunity and augments pro-inflammatory adaptive immunity. Thus, low vitamin-D stores could aggravate sarcoid inflammation while repletion of vitamin-D stores could mitigate inflammation in sarcoidosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcoidosis, Vitamin D Insufficiency

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Vitamin-D insufficient subjects will receive either vitamin D2 repletion or placebo Vitamin-D sufficient subjects will be observed without treatment.
Masking
ParticipantCare ProviderInvestigator
Masking Description
Groups separated by a) use / non-use of oral prednisone, and b) status of serum 25-hydroxy-vitamin-D level (sufficient or insufficient). Those who are vitamin-D insufficient will be randomized to receive either vitamin D2 or placebo.
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low vit-D, Ergocalciferol
Arm Type
Experimental
Arm Description
Low serum vitamin D level, split by use or non-use of systemic corticosteroid. Vitamin D2 (Ergocalciferol) 50,000 units will be given by mouth once a week for 12 weeks, then once a month for 12 weeks. Daily dietary requirement (calcium citrate with vitamin D2 (200 mg/250 Units tablets, 4 tablets per day) will be given by mouth for 24 weeks).
Arm Title
Low vit-D, Placebo
Arm Type
Placebo Comparator
Arm Description
Low serum vitamin D level, split by use or non-use of systemic corticosteroid. Placebo capsules of identical size and appearance will be given by mouth once a week for 12 weeks, then once a month for 12 weeks. Daily dietary requirement (calcium citrate with vitamin D2 (200 mg/250 Units tablets, 4 tablets per day) will be given by mouth for 24 weeks).
Arm Title
Normal vit-D, control
Arm Type
Other
Arm Description
Normal serum vitamin D level, split by use or non-use of systemic corticosteroid. Daily dietary requirement (calcium citrate with vitamin D2 (200 mg/250 Units tablets, 4 tablets per day) will be given by mouth for 24 weeks).
Intervention Type
Drug
Intervention Name(s)
Ergocalciferol
Other Intervention Name(s)
Vitamin D2
Intervention Description
Vitamin D2 50,000 units
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Placebo oral tablets
Intervention Description
Sugar pill manufactured to mimic ergocalciferol 50,000 units
Intervention Type
Drug
Intervention Name(s)
Calcium Citrate with Vitamin D2
Other Intervention Name(s)
Citracal
Intervention Description
To meet the recommended minimum daily dietary requirements
Primary Outcome Measure Information:
Title
Change in lung function from baseline
Description
(Measurement at end of study)/(measurement at enrollment)
Time Frame
Baseline and 24 weeks
Secondary Outcome Measure Information:
Title
Change in King's Sarcoidosis Questionnaire Score
Description
Standard validated questionnaire for assessing the impact of sarcoidosis on quality of life. Questions address symptoms, activities and psychosocial impacts of disease. It consists of 29 questions on general health, medications, and symptoms in lung, skin, and eyes, summed to derive a total score. Each question is scored on a scale of 1 (worst) to 7 (best). Minimum total score = 5 (poorest health). Maximum total score = 203 (best health).
Time Frame
Baseline, 12 and 24 weeks
Title
Change in six minute walk distance
Description
(Measurement at end of study)/(measurement at enrollment)
Time Frame
Baseline and 24 weeks
Title
Change in blood cell counts from complete blood count (CBC)
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in metabolic profile from complete metabolic panel (CMP)
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in serum vitamin-D metabolite concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in serum angiotensin converting enzyme (ACE) concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in serum serum gamma-globulin concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in serum C-reactive protein (CRP) concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in serum tumor Necrosis factor-alpha (TNF-alpha) concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in serum interferon-gamma (IFN-gamma) concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Changes in serum interleukin concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in 24 hour urine calcium/creatinine ratio
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in 24 hour urine deoxypyridinoline concentration
Description
(Measurement at study point)/(initial measurement at enrollment)
Time Frame
Baseline, 12 and 24 weeks
Title
Change in fractional lung tissue volume on computed/positron emission tomography (PET/CT)
Description
(Measurement at end of study)/(measurement at enrollment)
Time Frame
Baseline and 24 weeks
Title
Change in Fluoro-deoxyglucose (FDG) uptake on PET/CT
Description
(Measurement at end of study)/(measurement at enrollment
Time Frame
Baseline and 24 weeks
Title
Change in bone density z-score
Description
(Measurement at end of study)/(measurement at enrollment)
Time Frame
Baseline and 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Stable medical condition defined as no hospitalization or emergency room visit in the previous 3 months No evidence of active pulmonary or systemic infection No other active inflammatory disease, No active malignancy. Normal serum ionized calcium level Exclusion Criteria: Hospitalization or emergency room visit in the previous 3 months Evidence of active pulmonary or systemic infection Evidence of active other inflammatory disease Evidence of active malignancy Elevated serum ionized calcium level
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Connie Hsia, MD
Organizational Affiliation
University of Texas Southwestern Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas Southwestern Medical Center, and Parkland Health and Hospital System
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390-9034
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified participant data for primary and secondary outcome measures will be made available.
IPD Sharing Time Frame
Within 6 months of study completion
IPD Sharing Access Criteria
Data access requests will be reviewed by an external independent review panel. Requestors will be required to sign a Data Access Agreement.
Citations:
PubMed Identifier
27053725
Citation
Capolongo G, Xu LH, Accardo M, Sanduzzi A, Stanziola AA, Colao A, Agostini C, Zacchia M, Capasso G, Adams-Huet B, Moe OW, Maalouf NM, Sakhaee K, Hsia CC. Vitamin-D status and mineral metabolism in two ethnic populations with sarcoidosis. J Investig Med. 2016 Jun;64(5):1025-34. doi: 10.1136/jim-2016-000101. Epub 2016 Apr 6.
Results Reference
result
PubMed Identifier
15225842
Citation
Vieth R. Why the optimal requirement for Vitamin D3 is probably much higher than what is officially recommended for adults. J Steroid Biochem Mol Biol. 2004 May;89-90(1-5):575-9. doi: 10.1016/j.jsbmb.2004.03.038.
Results Reference
result
PubMed Identifier
24157819
Citation
Bolland MJ, Wilsher ML, Grey A, Horne AM, Fenwick S, Gamble GD, Reid IR. Randomised controlled trial of vitamin D supplementation in sarcoidosis. BMJ Open. 2013 Oct 23;3(10):e003562. doi: 10.1136/bmjopen-2013-003562.
Results Reference
result
PubMed Identifier
24753153
Citation
Kamphuis LS, Bonte-Mineur F, van Laar JA, van Hagen PM, van Daele PL. Calcium and vitamin D in sarcoidosis: is supplementation safe? J Bone Miner Res. 2014 Nov;29(11):2498-503. doi: 10.1002/jbmr.2262.
Results Reference
result

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Vitamin D Homeostasis in Sarcoidosis

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