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Antioxidant Therapy to Reduce Inflammation in Sickle Cell Disease

Primary Purpose

Anemia, Sickle Cell

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
alpha-lipoic acid and acetyl-L-carnitine
Control
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 Anemia, Sickle Cell focused on measuring Antioxidant, Inflammation, Sickle Cell Disease, Oxidative Stress, Cytokines, anti-inflammatory, Acetylcarnitine

Eligibility Criteria

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

Inclusion Criteria:

  • Proven diagnosis of sickle cell disease, either homozygous sickle disease or Hb S Beta zero thalassemia genotype
  • Age at entry at least 14 years. Younger children will not be included since the combination alpha-lipoic acid and acetyl-L-carnitine tablets are not available in a smaller dose at this time.

Exclusion Criteria:

  • More than 3 packed red blood transfusions in the past 12 months
  • Coexisting illness that could contribute to inflammation. These include chronic hepatitis, lupus, arthritis, inflammatory bowel disease, chronic osteomyelitis, and other similar conditions.
  • Acute sickle cell disease related symptoms requiring a hospital visit in the past 4 weeks
  • Women who are pregnant, attempting to get pregnant, or breast feeding
  • Active participation in other investigational drug or device studies
  • Participants who start hydroxyurea or regular transfusion therapy during the course of the study on the recommendation of their primary hematologist will be ineligible for further participation.

Sites / Locations

  • Children's Hospital & Research Center Oakland

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

alpha-lipoic acid and acetyl-L-carnitine

Placebo

Arm Description

alpha-lipoic acid and acetyl-L-carnitine1400 mg tablet twice a day for 6 months.

1400 mg placebo tablet twice a day for 6 months.

Outcomes

Primary Outcome Measures

C-Reactive Protein
C-Reactive Protein (CRP) was measured by a clinical laboratory. Measuring the quantity of serum CRP is helpful in recognizing inflammatory states.

Secondary Outcome Measures

Full Information

First Posted
January 20, 2010
Last Updated
July 13, 2021
Sponsor
UCSF Benioff Children's Hospital Oakland
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT01054768
Brief Title
Antioxidant Therapy to Reduce Inflammation in Sickle Cell Disease
Official Title
Antioxidant Therapy to Reduce Inflammation in Sickle Cell Disease
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
April 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
UCSF Benioff Children's Hospital Oakland
Collaborators
National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether alpha-lipoic acid and acetyl-L-carnitine will lower systemic inflammation in patients with Sickle Cell Disease by reducing oxidative stress, which will result in a decrease in the frequency of vaso-occlusive pain episodes and improve their quality of life.
Detailed Description
People with sickle cell disease have more inflammation (a response of body tissues to injury or irritation) than people without sickle cell disease. This inflammation can be measured in the blood by checking the level of a protein called C reactive protein as well as other changes we see in blood due to inflammation (such as changes in platelets and other cells). There is even more inflammation during sickle-related complications (like pain or acute chest syndrome). We want to test if inflammation in people with sickle cell disease can be reduced by the use of antioxidant compounds. Antioxidants are nutrients (certain vitamins, minerals and enzymes) that can counteract the effects of oxidative stress arising from free radicals in our cells. The formation of free radicals is a normal cell process, but uncontrolled oxidative stress can cause problems for us. One such harmful problem is inflammation. We know from other research studies that antioxidants help with some conditions related to inflammation. In this study the antioxidant being tested is a combination of alpha-lipoic acid and acetyl-L-carnitine, both of which are natural parts of many of the foods we eat and are needed by our cells to make energy from food.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia, Sickle Cell
Keywords
Antioxidant, Inflammation, Sickle Cell Disease, Oxidative Stress, Cytokines, anti-inflammatory, Acetylcarnitine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
37 (Actual)

8. Arms, Groups, and Interventions

Arm Title
alpha-lipoic acid and acetyl-L-carnitine
Arm Type
Experimental
Arm Description
alpha-lipoic acid and acetyl-L-carnitine1400 mg tablet twice a day for 6 months.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
1400 mg placebo tablet twice a day for 6 months.
Intervention Type
Drug
Intervention Name(s)
alpha-lipoic acid and acetyl-L-carnitine
Other Intervention Name(s)
Experimental
Intervention Description
none to report
Intervention Type
Drug
Intervention Name(s)
Control
Other Intervention Name(s)
Placebo
Intervention Description
none to report
Primary Outcome Measure Information:
Title
C-Reactive Protein
Description
C-Reactive Protein (CRP) was measured by a clinical laboratory. Measuring the quantity of serum CRP is helpful in recognizing inflammatory states.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Proven diagnosis of sickle cell disease, either homozygous sickle disease or Hb S Beta zero thalassemia genotype Age at entry at least 14 years. Younger children will not be included since the combination alpha-lipoic acid and acetyl-L-carnitine tablets are not available in a smaller dose at this time. Exclusion Criteria: More than 3 packed red blood transfusions in the past 12 months Coexisting illness that could contribute to inflammation. These include chronic hepatitis, lupus, arthritis, inflammatory bowel disease, chronic osteomyelitis, and other similar conditions. Acute sickle cell disease related symptoms requiring a hospital visit in the past 4 weeks Women who are pregnant, attempting to get pregnant, or breast feeding Active participation in other investigational drug or device studies Participants who start hydroxyurea or regular transfusion therapy during the course of the study on the recommendation of their primary hematologist will be ineligible for further participation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elliott Vichinsky, M.D.
Organizational Affiliation
UCSF Benioff Children's Hospital Oakland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bruce N. Ames, Ph.D.
Organizational Affiliation
UCSF Benioff Children's Hospital Oakland
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ashutosh Lal, M.D.
Organizational Affiliation
UCSF Benioff Children's Hospital Oakland
Official's Role
Study Director
Facility Information:
Facility Name
Children's Hospital & Research Center Oakland
City
Oakland
State/Province
California
ZIP/Postal Code
94609
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Antioxidant Therapy to Reduce Inflammation in Sickle Cell Disease

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