search
Back to results

Oral Contraceptives in the Metabolic Syndrome

Primary Purpose

Metabolic Syndrome X, Insulin Resistance, Obesity

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ortho Tri Cyclen
Sponsored by
Virginia Commonwealth University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Metabolic Syndrome X focused on measuring Inflammatory markers, oral contraceptions, obesity, metabolic syndrome X

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Acceptable health based on interview, medical history, physical examination, and laboratory tests (comprehensive metabolic panel - SMA20, and complete blood count - CBC); Have not taken oral contraceptives (OCs) in the past 3 months; Ability to comply with the requirements of the study; Ability and willingness to provide signed, witnessed informed consent. In addition, women with the metabolic syndrome must meet the National Cholesterol Education Program (NCEP) defined criteria of the metabolic syndrome, that is, having at least 3 of the 5 factors: increased waist circumference > 35 inches, hypertriglyceridemia ≥ 150 mg/dL, low high-density lipoprotein (HDL) cholesterol < 50 mg/dL in women, hypertension (≥ 130/≥ 85 mmHg), fasting glucose ≥ 100 mg/dL. Obese women with or without the metabolic syndrome should have a Body Mass Index (BMI) > 30 kg/m2 and lean women should have a Body Mass Index BMI < 25 kg/m2. Exclusion Criteria: Diabetes mellitus by fasting glucose or a 2-hour oral glucose tolerance test (OGTT); Clinically significant pulmonary, cardiac (including but not limited to ischemic heart disease, stable/unstable angina, and congestive heart failure), renal, hepatic, cholestatic, neurologic, psychiatric, infectious, and malignant disease (other than melanoma skin cancer); History of thromboembolism, myocardial infarction, cerebrovascular accident, vascular disease, known coagulopathy, prolonged immobilization, or recent major surgery (within past 6 months); Systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 100 mmHg (mild hypertension is not an exclusion criterion); History of breast cancer, migraine headaches, or age ≥ 35 years and smoker of ≥ 20 cigarettes/day; Use of metformin, thiazolidinediones, anti-hyperlipidemic drugs, anti-hypertensive drugs, glucocorticoids, or anti-androgens (spironolactone, flutamide, etc.) within 3 months; Documented or suspected illicit drug abuse or alcoholism within one year; Ingestion of any investigational drugs within 3 months prior to the study onset; and Pregnancy or lactation (≤ 6 weeks postpartum); Hematocrit < 33g/dL. These exclusion criteria are based on study requirements and also go beyond guidelines for OC use published by the World Health Organization.

Sites / Locations

  • Virginia Commonwealth University General Clinical Research Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Obese women with metabolic syndrome

Obese women without metabolic syndrome

lean women without metabolic syndrome

Arm Description

Outcomes

Primary Outcome Measures

Changes in Insulin Sensitivity Associated With Oral Contraceptive (OC) Use Compared Among (1) Obese Women and (2) Lean Women
Insulin sensitivity was assessed by frequent sampling intravenous glucose tolerance test (FSIVGTT).

Secondary Outcome Measures

Changes in Lipid Profile Compared Associated With OC Use Among (1) Obese Women and (2) Lean Women
The lipid profile is assessed through blood sample analysis for low-density lipoprotein (LDL), Triglycerides and high-density lipoprotein (HDL).
Inflammatory Marker Changes, High Sensitive C-reactive Protein (Hs-CRP) and Adiponectin, Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Inflammatory markers are assessed through blood analysis for C-reactive protein (hs-CRP) and adiponectin.
Changes in Estrogen Metabolites (Plasma) Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Changes in Waist-to-Hip Ratio Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Waist-to-hip ratio is assessed through calculated ratio of waist and hip circumference.
Inflammatory Marker Changes (MCP-1) Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Inflammatory marker is assessed through blood analysis for Monocyte chemotactic protein-1 (MCP-1).
Changes in Blood Pressure Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Changes in Body Mass Index (BMI) Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Body Mass Index is a calculation of height and weight: kg/m²
Changes in Waist Circumference Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Inflammatory Marker Changes, Soluble Vascular Cell Adhesion Molecule (sVCAM) and Soluble Intercellular Adhesion Molecule (sICAM), Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
These inflammatory markers are assessed through blood analysis of Soluble Vascular Cell Adhesion Molecule (sVCAM) and soluble intercellular adhesion molecule (sICAM).

Full Information

First Posted
September 13, 2005
Last Updated
July 10, 2018
Sponsor
Virginia Commonwealth University
search

1. Study Identification

Unique Protocol Identification Number
NCT00205504
Brief Title
Oral Contraceptives in the Metabolic Syndrome
Official Title
Oral Contraceptives in the Metabolic Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
June 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Virginia Commonwealth University

4. Oversight

5. Study Description

Brief Summary
Oral contraceptives (OCs) are the most widely used method of reversible birth control. However, the long-term cardiovascular safety of the widely used low-dose OCs (ethinyl-estradiol < 50 mcg) is still debated. Although cardiovascular events are rare in young women whether they use OCs or not, the risks of myocardial infarction and ischemic stroke are increased among users of OCs who have conventional cardiovascular risk factors such as use of tobacco, diabetes or hypercholesterolemia. However, the risk of cardiovascular events in OC users with emerging cardiovascular risk factors (such as obesity and the metabolic syndrome) have not been investigated. Recently, the metabolic syndrome has been linked with the risk of cardiovascular disease. The syndrome is a clustering of risk factors in a single individual, and its underlying cause may be insulin resistance. Whether the metabolic syndrome predicts a higher cardiovascular risk in OC users has not been studied. This is a critical problem because the metabolic syndrome is prevalent in 24% of adults. Until the cardiovascular risks in users of OC are clearly defined, the appropriate use of OC with the least harm would not be possible. The investigator's long-term goal is to understand the best way to prevent and treat cardiovascular disease in women. The objective of this particular project is to obtain pilot data on the extent to which the metabolic syndrome and obesity affects glucose metabolism and cardiovascular risks in women taking OCs. The researchers hypothesize that women with metabolic syndrome and obese women will have worsened glucose metabolism and elevated cardiovascular risks associated with OC use, when compared to normal weight women without the metabolic syndrome. Results of this study will clarify the risk factors for cardiovascular events in women taking OCs, and will serve as pilot data for a National Institutes of Health (NIH) proposal. Once the cardiovascular risk factors of OC users are understood, clinicians can make better informed decisions about contraceptive choices for their patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome X, Insulin Resistance, Obesity, Cardiovascular Diseases
Keywords
Inflammatory markers, oral contraceptions, obesity, metabolic syndrome X

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Obese women with metabolic syndrome
Arm Type
Active Comparator
Arm Title
Obese women without metabolic syndrome
Arm Type
Active Comparator
Arm Title
lean women without metabolic syndrome
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Ortho Tri Cyclen
Intervention Description
Ortho Tri Cyclen, one tablet daily, for 6 cycles
Primary Outcome Measure Information:
Title
Changes in Insulin Sensitivity Associated With Oral Contraceptive (OC) Use Compared Among (1) Obese Women and (2) Lean Women
Description
Insulin sensitivity was assessed by frequent sampling intravenous glucose tolerance test (FSIVGTT).
Time Frame
Baseline and 6 months
Secondary Outcome Measure Information:
Title
Changes in Lipid Profile Compared Associated With OC Use Among (1) Obese Women and (2) Lean Women
Description
The lipid profile is assessed through blood sample analysis for low-density lipoprotein (LDL), Triglycerides and high-density lipoprotein (HDL).
Time Frame
Baseline and 6 months
Title
Inflammatory Marker Changes, High Sensitive C-reactive Protein (Hs-CRP) and Adiponectin, Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Description
Inflammatory markers are assessed through blood analysis for C-reactive protein (hs-CRP) and adiponectin.
Time Frame
Baseline and 6 months
Title
Changes in Estrogen Metabolites (Plasma) Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Time Frame
Baseline and 6 months
Title
Changes in Waist-to-Hip Ratio Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Description
Waist-to-hip ratio is assessed through calculated ratio of waist and hip circumference.
Time Frame
Baseline and 6 months
Title
Inflammatory Marker Changes (MCP-1) Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Description
Inflammatory marker is assessed through blood analysis for Monocyte chemotactic protein-1 (MCP-1).
Time Frame
Baseline and 6 months
Title
Changes in Blood Pressure Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Time Frame
Baseline and 6 months
Title
Changes in Body Mass Index (BMI) Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Description
Body Mass Index is a calculation of height and weight: kg/m²
Time Frame
Baseline and 6 months
Title
Changes in Waist Circumference Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Time Frame
Baseline and 6 months
Title
Inflammatory Marker Changes, Soluble Vascular Cell Adhesion Molecule (sVCAM) and Soluble Intercellular Adhesion Molecule (sICAM), Associated With OC Use Compared Among (1) Obese Women and (2) Lean Women
Description
These inflammatory markers are assessed through blood analysis of Soluble Vascular Cell Adhesion Molecule (sVCAM) and soluble intercellular adhesion molecule (sICAM).
Time Frame
Baseline and 6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Acceptable health based on interview, medical history, physical examination, and laboratory tests (comprehensive metabolic panel - SMA20, and complete blood count - CBC); Have not taken oral contraceptives (OCs) in the past 3 months; Ability to comply with the requirements of the study; Ability and willingness to provide signed, witnessed informed consent. In addition, women with the metabolic syndrome must meet the National Cholesterol Education Program (NCEP) defined criteria of the metabolic syndrome, that is, having at least 3 of the 5 factors: increased waist circumference > 35 inches, hypertriglyceridemia ≥ 150 mg/dL, low high-density lipoprotein (HDL) cholesterol < 50 mg/dL in women, hypertension (≥ 130/≥ 85 mmHg), fasting glucose ≥ 100 mg/dL. Obese women with or without the metabolic syndrome should have a Body Mass Index (BMI) > 30 kg/m2 and lean women should have a Body Mass Index BMI < 25 kg/m2. Exclusion Criteria: Diabetes mellitus by fasting glucose or a 2-hour oral glucose tolerance test (OGTT); Clinically significant pulmonary, cardiac (including but not limited to ischemic heart disease, stable/unstable angina, and congestive heart failure), renal, hepatic, cholestatic, neurologic, psychiatric, infectious, and malignant disease (other than melanoma skin cancer); History of thromboembolism, myocardial infarction, cerebrovascular accident, vascular disease, known coagulopathy, prolonged immobilization, or recent major surgery (within past 6 months); Systolic blood pressure greater than 160 mmHg or diastolic blood pressure greater than 100 mmHg (mild hypertension is not an exclusion criterion); History of breast cancer, migraine headaches, or age ≥ 35 years and smoker of ≥ 20 cigarettes/day; Use of metformin, thiazolidinediones, anti-hyperlipidemic drugs, anti-hypertensive drugs, glucocorticoids, or anti-androgens (spironolactone, flutamide, etc.) within 3 months; Documented or suspected illicit drug abuse or alcoholism within one year; Ingestion of any investigational drugs within 3 months prior to the study onset; and Pregnancy or lactation (≤ 6 weeks postpartum); Hematocrit < 33g/dL. These exclusion criteria are based on study requirements and also go beyond guidelines for OC use published by the World Health Organization.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kai I Cheang, Pharm.D.
Organizational Affiliation
Virginia Commonwealth University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John E Nestler, M.D.
Organizational Affiliation
Virginia Commonwealth University
Official's Role
Study Director
Facility Information:
Facility Name
Virginia Commonwealth University General Clinical Research Center
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23298
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21676394
Citation
Cheang KI, Essah PA, Sharma S, Wickham EP 3rd, Nestler JE. Divergent effects of a combined hormonal oral contraceptive on insulin sensitivity in lean versus obese women. Fertil Steril. 2011 Aug;96(2):353-359.e1. doi: 10.1016/j.fertnstert.2011.05.039. Epub 2011 Jun 15.
Results Reference
result

Learn more about this trial

Oral Contraceptives in the Metabolic Syndrome

We'll reach out to this number within 24 hrs