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Problematic uterine bleeding after the insertion of the LNG IUS is a well documented side effect. The levonorgestrel intrauterine system (LNG IUS) was approved for treatment of heavy menstrual bleeding (HMB) by the FDA in October 2009. To reduce the incidence and severity of post-insertional uterine bleeding, pretreatment with norethindrone acetate may effectively slough the endometrium prior to insertion of the LNG IUS.
This study will examine whether or not pretreatment with oral norethindrone acetate prior to the insertion of a hormonal intrauterine device will affect post-insertional uterine bleeding. The subjects enrolling in the study will have documented heavy menstrual bleeding (HMB) and desire the levonorgestrel intrauterine system (LNG IUS) (Mirena®, Bayer, Inc. Pittsburgh, PA) for symptomatic relief. HMB for this study is defined as heavy bleeding at regular intervals at least 20-40 days apart. Subjects will be randomized to one of two groups. One group will receive norethindrone acetate for two consecutive months prior to LNG IUS insertion while the other group will proceed with direct insertion of the LNG IUS with no hormonal pre-treatment. Subjects will be followed for a period of 180 days post LNG IUS insertion. Bleeding patterns will be recorded daily.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Norethindrone acetate pretreatment | Active Comparator | This arm will receive two cycles of norethindrone acetate before LVN IUS insertion. |
|
| No pretreatment | Other | LVN IUS is placed without norethindrone acetate pretreatment. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Norethindrone acetate pretreatment | Drug | 5 mg tablets, three times a day for 21 days for 2 menstrual cycles. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Total number of bleeding days | Number of days on study calendars with menstrual flow | up to 180 days |
| Measure | Description | Time Frame |
|---|---|---|
| Menorrhagia Questionnaire | Patients will assess the impact of their menstrual bleeding on their lifestyle. | up to 180 days |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Wendy M White, CCRP | Contact | 254-724-8301 | wewhite@swmail.sw.org |
| Name | Affiliation | Role |
|---|---|---|
| Patricia J Sulak, MD | Scott and White Hospital & Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Scott and White Hospital and Clinic | Recruiting | Temple | Texas | 76508 | United States |
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| No pretreatment | Other | LVN IUS is placed withour Norethindrone acetate pretreatment. |
|
| ID | Term |
|---|---|
| D008595 | Menorrhagia |
| ID | Term |
|---|---|
| D014592 | Uterine Hemorrhage |
| D014591 | Uterine Diseases |
| D005831 | Genital Diseases, Female |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D000091662 | Genital Diseases |
| D006470 | Hemorrhage |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D008599 | Menstruation Disturbances |
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| ID | Term |
|---|---|
| D000077563 | Norethindrone Acetate |
| ID | Term |
|---|---|
| D009640 | Norethindrone |
| D009652 | Norpregnenes |
| D009650 | Norpregnanes |
| D009654 | Norsteroids |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
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