search
Back to results

Zinc & Bone Health in Thalassemia: The Think Zinc Study (ThinkZn)

Primary Purpose

Thalassemia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Zinc
Placebo
Sponsored by
UCSF Benioff Children's Hospital Oakland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Thalassemia focused on measuring zinc, thalassemia, bone mineral density

Eligibility Criteria

6 Years - 30 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 6 to 30 years of age
  • thalassemia
  • bone mineral density Z-score < -1.0 (by DXA)

Exclusion Criteria:

  • Bone marrow transplant recipient
  • Currently prescribed treatment for low bone mass other than calcium or vitamin D (e.g. calcitonin, bisphosphonates)
  • Currently prescribed zinc supplementation who are unable or unwilling to stop during this trial
  • Currently participating in another trial with a medication known to affect bone mineral density.
  • Chronic use of systemic corticosteroids
  • Untreated hypogonadism or growth hormone deficiency
  • Baseline serum copper < 70 µg/dL
  • Baseline vitamin D-25OH < 11 ng/mL
  • Pregnant or lactating at study entry

Sites / Locations

  • Children's Hospital & Research Center, Oakland
  • University of California, San Francisco
  • Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo Capsule

Zinc (25 mg/d)

Arm Description

placebo capsule, similar in size, shape and color to zinc capsule, taken once daily for 18 months

25 mg of elemental Zinc as zinc sulphate taken once daily for 18 months

Outcomes

Primary Outcome Measures

Change in Lumbar Spine Bone Mineral Density (BMD) by DXA (Baseline to 18 Months)
Change in pa spine bone mineral density by DXA between baseline and 18 months
Change in Whole Body Bone Mineral Content (BMC) by DXA (Baseline to 18 Months)

Secondary Outcome Measures

Osteocalcin, a Marker of Bone Formation
Absolute change in serum osteocalcin between 0 and 18 months, intention to treat analysis between the zinc and placebo groups

Full Information

First Posted
April 11, 2007
Last Updated
December 3, 2020
Sponsor
UCSF Benioff Children's Hospital Oakland
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), Children's Hospital of Philadelphia, University of California, San Francisco
search

1. Study Identification

Unique Protocol Identification Number
NCT00459732
Brief Title
Zinc & Bone Health in Thalassemia: The Think Zinc Study
Acronym
ThinkZn
Official Title
Zinc and Bone Metabolism in Thalassemia
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
April 2006 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
February 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
UCSF Benioff Children's Hospital Oakland
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), Children's Hospital of Philadelphia, University of California, San Francisco

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to test whether zinc can improve bone health in young patients with thalassemia.
Detailed Description
The primary aim of this study is to determine if zinc supplementation improves bone health in young patients with thalassemia. Osteoporosis is a significant co-morbidity in patients with thalassemia which leads to decreased quality of life. The most effective way to prevent osteoporosis is to build strong, dense bones in the early years. A combination of disease, endocrine and nutritional factors likely contribute to the etiology of osteoporosis in this population. However, even well transfused patients with normal gonadal function who are supplemented with calcium have low bone mass. It is hypothesized that patients with thalassemia have low bone mass, in part, due to zinc deficiency. Sub-optimal zinc status has been identified in patients with thalassemia and zinc supplementation has been shown to improve linear growth. To test the primary hypothesis, an 18 month randomized placebo-controlled trial of zinc supplementation (25 mg Zn/day) vs. placebo will be conducted in 60 young patients (6-30 yrs) with thalassemia and low bone mass (spine BMD Z-score <-1.0). Bone health, as estimated from measurements of bone mass (by DXA and pQCT) and markers of bone formation and resorption will be the primary outcome variables. This will be the first study to examine the effects of zinc. supplementation on bone health in patients with thalassemia. If zinc supplementation is found to have a clinically important effect, this simple, safe, non-invasive therapy could quickly become a part of the standard care of these young patients and improve overall health in children and adult patients with thalassemia

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thalassemia
Keywords
zinc, thalassemia, bone mineral density

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo Capsule
Arm Type
Placebo Comparator
Arm Description
placebo capsule, similar in size, shape and color to zinc capsule, taken once daily for 18 months
Arm Title
Zinc (25 mg/d)
Arm Type
Active Comparator
Arm Description
25 mg of elemental Zinc as zinc sulphate taken once daily for 18 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Zinc
Other Intervention Name(s)
zinc sulphate, elemental zinc
Intervention Description
25 mg of elemental zinc as zinc sulphate take once daily for 18 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Other Intervention Name(s)
"sugar" pill
Intervention Description
Placebo capsule, identical to the zn capsule in size, shape and color, taken once daily for 18 months
Primary Outcome Measure Information:
Title
Change in Lumbar Spine Bone Mineral Density (BMD) by DXA (Baseline to 18 Months)
Description
Change in pa spine bone mineral density by DXA between baseline and 18 months
Time Frame
0 to 18 months
Title
Change in Whole Body Bone Mineral Content (BMC) by DXA (Baseline to 18 Months)
Time Frame
Baseline to 18 months
Secondary Outcome Measure Information:
Title
Osteocalcin, a Marker of Bone Formation
Description
Absolute change in serum osteocalcin between 0 and 18 months, intention to treat analysis between the zinc and placebo groups
Time Frame
Baseline to 18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 6 to 30 years of age thalassemia bone mineral density Z-score < -1.0 (by DXA) Exclusion Criteria: Bone marrow transplant recipient Currently prescribed treatment for low bone mass other than calcium or vitamin D (e.g. calcitonin, bisphosphonates) Currently prescribed zinc supplementation who are unable or unwilling to stop during this trial Currently participating in another trial with a medication known to affect bone mineral density. Chronic use of systemic corticosteroids Untreated hypogonadism or growth hormone deficiency Baseline serum copper < 70 µg/dL Baseline vitamin D-25OH < 11 ng/mL Pregnant or lactating at study entry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ellen B. Fung, PhD, RD
Organizational Affiliation
UCSF Benioff Children's Hospital Oakland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital & Research Center, Oakland
City
Oakland
State/Province
California
ZIP/Postal Code
94609
Country
United States
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23945720
Citation
Fung EB, Kwiatkowski JL, Huang JN, Gildengorin G, King JC, Vichinsky EP. Zinc supplementation improves bone density in patients with thalassemia: a double-blind, randomized, placebo-controlled trial. Am J Clin Nutr. 2013 Oct;98(4):960-71. doi: 10.3945/ajcn.112.049221. Epub 2013 Aug 14.
Results Reference
derived

Learn more about this trial

Zinc & Bone Health in Thalassemia: The Think Zinc Study

We'll reach out to this number within 24 hrs