Eto BMI: The Effect of Body Mass Index on Etonogestrel Hormone Levels in Women Using the Single-rod Contraceptive Implant

Sponsor
Columbia University (Other)
Overall Status
Completed
CT.gov ID
NCT01855620
Collaborator
(none)
52
1
14.9
3.5

Study Details

Study Description

Brief Summary

Two-thirds of young women in the United States are overweight or obese. This excess weight may affect how their body metabolizes drugs such as different birth control methods. There is a not a lot of research about how excess weight could affect the hormone levels of the contraceptive implant. Methods like the implant contain only progesterone, which is a hormone that does not increase a woman's risk of blood clot. These methods would be preferred for overweight and obese women because excess weight also increases a woman's risk of blood clot.

The investigators propose a study comparing blood hormone levels of women using the implant for at least twelve months and in all weight categories. The investigators hope to show that all women, regardless of weight, will have hormone levels high enough to prevent pregnancy.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Two-thirds of reproductive-age women in the United States are either overweight or obese. Body composition may affect contraceptive hormone metabolism and possibly efficacy. Phase III studies to date included few women weighing more than 70 kilograms (134 of 923, 14.5%); there were no reported pregnancies in that group. Data about pregnancy rates for women in higher body mass index (BMI) categories using the etonogestrel implant exists, but we know little about how weight affects the serum etonogestrel levels. Progestin-only methods, such as the etonogestrel implant, may be preferred over combined methods including estrogens because obesity increases thrombosis risk.

    The investigators propose a prospective study to compare serum etonogestrel levels in the second and third years of implant use between women across body mass index categories.

    Based on previous studies, the investigators expect a difference in etonogestrel levels based on body weight; however, the investigators hypothesize that etonogestrel levels will remain above the threshold for ovulation suppression through three years of implant use for women across BMI categories.

    The investigators will measure the serum levels of etonogestrel in normal weight (BMI < 25kg/m2), overweight (BMI ≥ 25kg/m2 and < 30kg/m2), and obese women (BMI ≥ 30kg/m2) using the single-rod contraceptive implant for at least twelve months. Their primary objective is to compare the three groups and to evaluate whether etonogestrel levels fall below the critical level for contraceptive efficacy (90 pg/mL) (Díaz 1991) in any group.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    52 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Effect of Body Mass Index on Etonogestrel Levels in Women Using the Single-rod Contraceptive Implant
    Study Start Date :
    Dec 1, 2012
    Actual Primary Completion Date :
    Nov 1, 2013
    Actual Study Completion Date :
    Mar 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Normal weight women

    Women with implant for more than twelve months who have BMI <25.

    Overweight women

    Women with implant for more than twelve months who have BMI > or = 25 and <30.

    Obese women

    Women with implant for more than twelve months who have BMI > or = 30.

    Outcome Measures

    Primary Outcome Measures

    1. Serum Etonogestrel Level [Up to 12 months]

      The investigators will measure the serum levels of etonogestrel in normal weight (BMI < 25kg/m2), overweight (BMI ≥ 25kg/m2 and < 30kg/m2), and obese women (BMI ≥ 30kg/m2) using the single-rod contraceptive implant for at least twelve months. The primary objective is to compare the three groups and to evaluate whether etonogestrel levels fall below the critical level for contraceptive efficacy (90 pg/mL) (Díaz 1991) in any group.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Woman using contraceptive implant for more than 12 months

    • English or Spanish-speaking

    Exclusion Criteria:
    • None

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Columbia University Medical Center New York New York United States 10032

    Sponsors and Collaborators

    • Columbia University

    Investigators

    • Principal Investigator: Kathleen M Morrell, MD, Columbia University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Kathleen M. Morrell, Assistant Professor of Clinical Obgyn, Columbia University
    ClinicalTrials.gov Identifier:
    NCT01855620
    Other Study ID Numbers:
    • AAAK6606
    First Posted:
    May 16, 2013
    Last Update Posted:
    Apr 14, 2014
    Last Verified:
    Apr 1, 2014
    Keywords provided by Kathleen M. Morrell, Assistant Professor of Clinical Obgyn, Columbia University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 14, 2014