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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00487877
Other study ID # TASMC-06-NV-380-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received June 18, 2007
Last updated June 18, 2007
Start date June 2007
Est. completion date December 2007

Study information

Verified date December 2006
Source Tel-Aviv Sourasky Medical Center
Contact Nachum Vaisman, Prof.
Phone +972-524-266-596
Email vaisman@tasmc.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

To investigate the relationship between hungry-satiation situation including meal time and metabolism, skin temerature changing, simpathetic & para-simpathetic response To investigate the relashionship between hungry-satiation situation including meal time and heart rate


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Over 18 years old

2. BMI: 22-30 Kg / m2

Exclusion Criteria:

1. Any unbalanced chronic disease

2. Any infection disease

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Device:
SenseWear Pro3 Armband

i-button DS2191 H


Locations

Country Name City State
Israel The Unit of clinical Nutrition Tel Aviv

Sponsors (1)

Lead Sponsor Collaborator
Tel-Aviv Sourasky Medical Center

Country where clinical trial is conducted

Israel,