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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01297426
Other study ID # ENDA-013-10F
Secondary ID
Status Withdrawn
Phase N/A
First received February 14, 2011
Last updated December 23, 2015
Start date April 2011
Est. completion date June 2015

Study information

Verified date December 2015
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

Obesity does not respond to high circulating levels of the hormone leptin. This study is aiming at finding out why this happens and open new avenues for treatment of obesity.


Description:

Ex vivo and in vitro identification and study of leptin signaling pathways in commercially available cell lines serum/ plasma samples and discarded tissues from humans.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- men and women

- ages 18 to 65

- BMI ranges between 20 and 45 kg/m2

Exclusion Criteria:

- subjects requiring special diets

- history of illness other than obesity of diabetes

- taking medications known to influence glucose metabolism

- subjects with history of anaphylactic reaction or hypersensitivity to e. coli derived proteins or anesthetic agents

- women who are breastfeeding, pregnant or wanting to become pregnant

- subjects with bleeding dyscrasia or poor wound healing

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
United States VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Westerns / activation of signaling pathways (uo to two hours after treatment) 04/01/2016 No
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