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Study of Beet Juice for Patients With Sickle Cell Anemia

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02162225
Recruitment Status : Withdrawn (Enrollment was very slow. Hope to reopen as multi-site study)
First Posted : June 12, 2014
Last Update Posted : August 2, 2018
Sponsor:
Collaborators:
Wake Forest University
National Heart, Lung, and Blood Institute (NHLBI)
Information provided by (Responsible Party):
Wake Forest University Health Sciences

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.

Condition or disease Intervention/treatment Phase
Sickle Cell Anemia Drug: beet juice (Unbeetable) Phase 2

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.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase 2 Study of Effects of Plasma Nitrite in Sickle Cell Anemia
Study Start Date : September 2014
Estimated Primary Completion Date : February 2019
Estimated Study Completion Date : April 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Anemia

Arm Intervention/treatment
Experimental: Beet Juice

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.

Drug: beet juice (Unbeetable)

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 Measures :
  1. Total Number of Participants with Adverse Events as a Measure of Safety and Tolerability as a function of time [ Time Frame: up to 58 Days ]
    Physical symptoms will be assessed either by telephone or in person


Secondary Outcome Measures :
  1. Changes in Red blood cell properties as a function of time [ Time Frame: Days 1, 14, 28 ]
    Blood will be drawn and used to measure red blood cell deformability and mean corpuscular hemoglobin concentration

  2. Changes in Platelet function as a function of time [ Time Frame: Days 1, 14, 28 ]
    Blood will be drawn and used to measure platelets activation and aggregation



Information from the National Library of Medicine

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Ages Eligible for Study:   19 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02162225


Locations
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United States, North Carolina
Wake Forest University School of Medicine
Winston-Salem, North Carolina, United States, 27157
Sponsors and Collaborators
Wake Forest University Health Sciences
Wake Forest University
National Heart, Lung, and Blood Institute (NHLBI)
Investigators
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Principal Investigator: Natalia Dixon, MD Wake Forest University Health Sciences
Study Director: Daniel B Kim-Shapiro, PhD Wake Forest University
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Responsible Party: Wake Forest University Health Sciences
ClinicalTrials.gov Identifier: NCT02162225    
Other Study ID Numbers: Wake-58091
R37HL058091 ( U.S. NIH Grant/Contract )
First Posted: June 12, 2014    Key Record Dates
Last Update Posted: August 2, 2018
Last Verified: July 2018

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Wake Forest University Health Sciences:
Erythrocyte Deformability
Platelet Activation
Platelet Aggregation
Nitrite
Sickle Cell Anemia
Diet Therapy
Additional relevant MeSH terms:
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Anemia
Anemia, Sickle Cell
Hematologic Diseases
Anemia, Hemolytic, Congenital
Anemia, Hemolytic
Hemoglobinopathies
Genetic Diseases, Inborn