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Study of Beet Juice for Patients With Sickle Cell Anemia

Primary Purpose

Sickle Cell Anemia

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
beet juice (Unbeetable)
Sponsored by
Wake Forest University Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sickle Cell Anemia focused on measuring Erythrocyte Deformability, Platelet Activation, Platelet Aggregation, Nitrite, Sickle Cell Anemia, Diet Therapy

Eligibility Criteria

19 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • diagnosis of sickle cell anemia (Hb S/S or Hb S/beta thal0)
  • no acute illness at the time of obtaining the study
  • willingness to adhere to the study preparatory procedures including drinking the beet juice product daily
  • willingness to give consent in order to participate

Exclusion Criteria:

  • less than 19 years in age or older than 65
  • smoke or chew tobacco
  • currently take medications that affect stomach pH
  • atrophic gastritis
  • hypo-or hyperthyroidism
  • Type I or II diabetes
  • history of gout, kidney stones or hypotension
  • pregnant
  • aversion to the study-related testing procedures
  • allergy, sensitivity or aversion to the study beetroot juice beverage
  • suffered an acute sickle cell episode (involving hospitalization or a visit to the emergency room) within the past six months

Sites / Locations

  • Wake Forest University School of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Beet Juice

Arm Description

Volunteers will drink a single 8 ounce bottle of beet juice (Unbeetable) per day for 28 days. On days 1,14, and 28, the juice will be drunk just prior to having blood drawn. Blood will also be drawn 1.5 hours after drinking the juice on days 1,14, and 28.

Outcomes

Primary Outcome Measures

Total Number of Participants with Adverse Events as a Measure of Safety and Tolerability as a function of time
Physical symptoms will be assessed either by telephone or in person

Secondary Outcome Measures

Changes in Red blood cell properties as a function of time
Blood will be drawn and used to measure red blood cell deformability and mean corpuscular hemoglobin concentration
Changes in Platelet function as a function of time
Blood will be drawn and used to measure platelets activation and aggregation

Full Information

First Posted
June 9, 2014
Last Updated
July 31, 2018
Sponsor
Wake Forest University Health Sciences
Collaborators
Wake Forest University, National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT02162225
Brief Title
Study of Beet Juice for Patients With Sickle Cell Anemia
Official Title
Phase 2 Study of Effects of Plasma Nitrite in Sickle Cell Anemia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Withdrawn
Why Stopped
Enrollment was very slow. Hope to reopen as multi-site study
Study Start Date
September 2014 (undefined)
Primary Completion Date
February 2019 (Anticipated)
Study Completion Date
April 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences
Collaborators
Wake Forest University, National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators hypothesize that increasing plasma nitrite using dietary nitrate will improve platelet function and red cell deformability and decrease MCHC in patients with sickle cell disease. The investigators will test this hypothesis through administration of daily intake of beetroot juice (Unbeetable - Performance Drink) to patients with sickle cell disease for 28 days. The investigators will evaluate the safety of daily beet root juice intake in patients with sickle cell disease. In addition, the investigators will measure MCHC, red cell deformability, and platelet function (activation and aggregation) in response to daily intake of beet root juice in this patient population.
Detailed Description
Sickle cell disease is caused by dysfunction of a mutant form of hemoglobin which polymerizes under hypoxic conditions, sickling the red blood cell. Sickling makes the cells rigid which contributes to vascular occlusion and much morbidity and mortality. Cycles of sickling and unsickling leads to calcium (Ca) influx which activates the gardos channel which pumps out potassium from the cells. Loss of potassium leads to dehydration, poor deformability, and increased mean corpuscular hemoglobin concentration (MCHC) in red blood cells. Increased MCHC leads to increased polymerization. Thus, a significant therapeutic goal for sickle cell disease has been to decrease MCHC by blocking the Ca-influx induced dehydration. Rifkind and coworkers have shown that the NO+ donor sodium nitrosoprusside (SNP) can block Ca-induced loss of deformability when normal red blood cells are exposed to Ca and a Ca ionophore. The investigators have preliminary data showing that both NO activity donors SNP and nitrite can partially relieve loss of deformability due to cycles of sickling and unsickling in red cells from patients with sickle cell disease. Low nitric oxide (NO) bioavailabilty secondary to red cell hemolysis has been proposed to contribute to pathology in sickle cell disease. Low NO could lead to poor protection against Ca-induced potassium loss described above. Another consequence of low NO is likely to be increased platelet activation; sickle cell disease is pro-thrombotic disease. NO reduces platelet aggregation and activation. It has been shown that an acute dietary nitrate intervention can reduce platelet aggregation in healthy volunteers. Nitrate is converted to nitrite which is converted to NO in the body.6 Improved platelet function is likely due to increasing NO bioavailability through the nitrate intervention. In this pilot study, the safety of Beet Juice intake in patients with sickle cell disease will be evaluated using a self-administered health survey. Physiological effects of the Beet Juice will also be examined and the investigators hypothesize that increasing plasma nitrite using dietary nitrate will improve platelet function and red cell deformability and decrease MCHC in patients with sickle cell disease. The investigators will test this hypothesis through administration of daily intake of Beet Juice to patients with sickle cell disease for 28 days. The investigators will measure MCHC, red cell deformability, and platelet function (activation and aggregation) in response to the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sickle Cell Anemia
Keywords
Erythrocyte Deformability, Platelet Activation, Platelet Aggregation, Nitrite, Sickle Cell Anemia, Diet Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Beet Juice
Arm Type
Experimental
Arm Description
Volunteers will drink a single 8 ounce bottle of beet juice (Unbeetable) per day for 28 days. On days 1,14, and 28, the juice will be drunk just prior to having blood drawn. Blood will also be drawn 1.5 hours after drinking the juice on days 1,14, and 28.
Intervention Type
Drug
Intervention Name(s)
beet juice (Unbeetable)
Intervention Description
Volunteers will drink a single 8 ounce bottle of beet juice (Unbeetable) per day for 28 days. On days 1,14, and 28, the juice will be drunk just prior to having blood drawn. Blood will also be drawn 1.5 hours after drinking the juice on days 1,14, and 28.
Primary Outcome Measure Information:
Title
Total Number of Participants with Adverse Events as a Measure of Safety and Tolerability as a function of time
Description
Physical symptoms will be assessed either by telephone or in person
Time Frame
up to 58 Days
Secondary Outcome Measure Information:
Title
Changes in Red blood cell properties as a function of time
Description
Blood will be drawn and used to measure red blood cell deformability and mean corpuscular hemoglobin concentration
Time Frame
Days 1, 14, 28
Title
Changes in Platelet function as a function of time
Description
Blood will be drawn and used to measure platelets activation and aggregation
Time Frame
Days 1, 14, 28

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of sickle cell anemia (Hb S/S or Hb S/beta thal0) no acute illness at the time of obtaining the study willingness to adhere to the study preparatory procedures including drinking the beet juice product daily willingness to give consent in order to participate Exclusion Criteria: less than 19 years in age or older than 65 smoke or chew tobacco currently take medications that affect stomach pH atrophic gastritis hypo-or hyperthyroidism Type I or II diabetes history of gout, kidney stones or hypotension pregnant aversion to the study-related testing procedures allergy, sensitivity or aversion to the study beetroot juice beverage suffered an acute sickle cell episode (involving hospitalization or a visit to the emergency room) within the past six months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Natalia Dixon, MD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Daniel B Kim-Shapiro, PhD
Organizational Affiliation
Wake Forest University
Official's Role
Study Director
Facility Information:
Facility Name
Wake Forest University School of Medicine
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States

12. IPD Sharing Statement

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Study of Beet Juice for Patients With Sickle Cell Anemia

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