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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00454623
Other study ID # 06041EX
Secondary ID
Status Active, not recruiting
Phase N/A
First received March 29, 2007
Last updated March 30, 2007
Start date March 2006
Est. completion date June 2007

Study information

Verified date March 2007
Source The Cooper Health System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of the study is to establish the normal levels of the hormone adiponectin in women. Adiponectin is a newly discovered hormone, which is said to be associated with many changes in the human body and metabolism. The researchers aim is to establish the normal levels of this hormone. Hence, the researchers can identify people with abnormal levels who may be at risk of diseases and can do more studies to help them.


Description:

The prevalence of obesity has increased dramatically in recent years . It is commonly associated with type 2 diabetes, coronary artery disease, and hypertension, and the coexistence of these diseases has been termed the metabolic syndrome. White Adipose Tissue (WAT) has been increasingly recognized as an important endocrine organ that secretes a number of biologically active “adipokines” . Of these adipokines, adiponectin has recently attracted much attention because of its antidiabetic and antiatherogenic effects and is expected to be a novel therapeutic tool for diabetes and the metabolic syndrome . Adiponectin directly regulates glucose metabolism and insulin sensitivity by activation of AMPK.

Adiponectin expression is reduced in obese, insulin-resistant rodent models. Plasma adiponectin levels are also decreased in an obese rhesus monkey model that frequently develops type 2 diabetes. Levels have also been reported to be reduced in obese humans, particularly those with visceral obesity, and to correlate inversely with insulin resistance. Prospective and longitudinal studies have shown that lower adiponectin levels are associated with a higher incidence of diabetes.

Hypoadiponectinemia has been demonstrated to be independently associated with the metabolic syndrome. Reduced plasma adiponectin levels are also commonly observed in a variety of states frequently associated with insulin resistance, such as cardiovascular disease, ischemic heart disease, and hypertension. In women, lower adiponectin levels were associated with breast cancer, endometrial cancer, and polycystic ovarian syndrome.

By establishing normal serum levels of Adiponectin, researchers will be able to demonstrate deviations from the norm associated with investigated diseases and variables. When applied to pregnancy, it will help identify obstetrical complications associated with abnormal levels.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 300
Est. completion date June 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 40 Years
Eligibility Inclusion Criteria:

1. Age: 15 - 40 years old.

2. BMI: 18.5 - 24.9

3. No medical or chronic health problems.

4. If pregnant, singleton.

5. First blood sample can be obtained before 13 weeks gestation.

6. Plans to continue pregnancy till term and deliver at our hospital

Exclusion Criteria:

1. Hypertension.

2. Diabetes Mellitus.

3. Ischemic heart disease.

4. Metabolic disorders e.g. hyperlipidemia, hypercholesterolemia.

5. Endocrinological diseases e.g. thyroid or adrenal diseases.

6. Chronic Debilitating diseases e.g. SLE, or Cancer.

7. BMI less than18.5 or greater than 25.

8. Anorexia or Bulimia.

9. Polycystic ovarian disease.

10. In pregnant group:

1. Multiple gestations.

2. Hyperemesis or dehydration.

3. History of Gestational Diabetes, Preeclampsia, or other complications with previous pregnancies

4. If abnormal weight gain during pregnancy, will continue in the study but would not be included in establishing normal levels.

Study Design

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


Related Conditions & MeSH terms


Intervention

Behavioral:
drawing serum adiponectin level


Locations

Country Name City State
United States Cooper University Hospital Camden New Jersey

Sponsors (1)

Lead Sponsor Collaborator
The Cooper Health System

Country where clinical trial is conducted

United States, 

References & Publications (1)

Cseh K, Baranyi E, Melczer Z, Kaszás E, Palik E, Winkler G. Plasma adiponectin and pregnancy-induced insulin resistance. Diabetes Care. 2004 Jan;27(1):274-5. — View Citation

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