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The Effect of Dates on Plasma Lipids, Oxidative Stress and the Atherogenicity of Serum in Healthy Adults

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified September 2008 by HaEmek Medical Center, Israel.
Recruitment status was:  Not yet recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00750789
First Posted: September 11, 2008
Last Update Posted: September 11, 2008
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.
Information provided by:
HaEmek Medical Center, Israel
  Purpose
It has been proven in in-vitro studies that dates decrease the oxidative stress in serum. There have been no in-vivo studies to this date. The current study aims to test whether dates consumption by healthy adults decreases serum oxidative stress and improves serum PON1 activity and serum lipid profile.

Condition Intervention Phase
Atherosclerosis Dietary Supplement: dates Phase 4

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Prevention

Further study details as provided by HaEmek Medical Center, Israel:

Primary Outcome Measures:
  • serum oxidative stress [ Time Frame: 30 days ]

Secondary Outcome Measures:
  • serum lipid profile [ Time Frame: 30 days ]

Estimated Enrollment: 10
Study Start Date: September 2008
Estimated Primary Completion Date: November 2008 (Final data collection date for primary outcome measure)
Intervention Details:
    Dietary Supplement: dates
    5 maedjool dates or 7 emery dates per day for 2 weeks each with a washout period of 2 weeks between
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy volunteers

Exclusion Criteria:

  Contacts and Locations
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): NCT00750789


Contacts
Contact: Wasseem Rock, MD 04-6495135 wasseem_rock@yahoo.com

Locations
Israel
Emek Medical Center Not yet recruiting
Afula, Israel
Contact: Wasseem Rock, MD    04-6495135      
Sponsors and Collaborators
HaEmek Medical Center, Israel
Investigators
Principal Investigator: Wasseem Rock Emek Medical Center
  More Information

Responsible Party: Wasseem Rock, emek medical center
ClinicalTrials.gov Identifier: NCT00750789     History of Changes
Other Study ID Numbers: 0061-08-EMC
First Submitted: August 17, 2008
First Posted: September 11, 2008
Last Update Posted: September 11, 2008
Last Verified: September 2008

Additional relevant MeSH terms:
Atherosclerosis
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases