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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00750789
Other study ID # 0061-08-EMC
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received August 17, 2008
Last updated September 10, 2008
Start date September 2008

Study information

Verified date September 2008
Source HaEmek Medical Center, Israel
Contact Wasseem Rock, MD
Phone 04-6495135
Email wasseem_rock@yahoo.com
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 10
Est. completion date
Est. primary completion date November 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Healthy volunteers

Exclusion Criteria:

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
dates
5 maedjool dates or 7 emery dates per day for 2 weeks each with a washout period of 2 weeks between

Locations

Country Name City State
Israel Emek Medical Center Afula

Sponsors (1)

Lead Sponsor Collaborator
HaEmek Medical Center, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary serum oxidative stress 30 days No
Secondary serum lipid profile 30 days No
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