Measurements of Skin Physiological Parameters as Mean of Metabolic Assessment

NCT ID: NCT00487877

Last Updated: 2007-06-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-06-30

Study Completion Date

2007-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hungry-Satiation Situation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

NONE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

SenseWear Pro3 Armband

Intervention Type DEVICE

i-button DS2191 H

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Over 18 years old
2. BMI: 22-30 Kg / m2

Exclusion Criteria

1. Any unbalanced chronic disease
2. Any infection disease
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Tel-Aviv Sourasky Medical Center

OTHER_GOV

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Nachum Vaisman, Prof.

Role: PRINCIPAL_INVESTIGATOR

unaffiliation

Nachum Vaisman, Prof.

Role: PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

The Unit of clinical Nutrition

Tel Aviv, , Israel

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Israel

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Nachum Vaisman, Prof.

Role: CONTACT

+972-524-266-596

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Nachum Vaisman, Prof.

Role: primary

+972-524-266-596

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

TASMC-06-NV-380-CTIL

Identifier Type: -

Identifier Source: org_study_id