Brief Summary
The Essure procedure, FDA approved since 2002 and CE Mark approved since 2001, is the first permanent birth control method that can be performed in the comfort of a physician's office without hormones, cutting, burning or the risks associated with general anesthesia or tubal ligation. Soft, flexible inserts are placed in a woman's fallopian tubes through the cervix without incisions. Over the next three months, the body forms a natural barrier around the micro-inserts to prevent sperm from reaching the egg. Three months after the Essure procedure, a doctor performs an Essure Confirmation Test. In the United States, this test is called a hysterosalpingogram and evaluates the location of the inserts and whether the fallopian tubes are blocked. Outside of the United States, a standard x-ray is performed to evaluate the location of the inserts.
The purpose of this study is to evaluate whether a transvaginal ultrasound is an effective method of confirming micro-insert location.
The purpose of this study is to evaluate whether a transvaginal ultrasound is an effective method of confirming micro-insert location.
Brief Title
Essure Transvaginal Ultrasound (TVU) Study
Detailed Description
This study has previously been posted by Conceptus, Inc. (USA).
After acquiring Conceptus, Inc., Bayer HealthCare AG (Germany) is the sponsor of the trial.
After acquiring Conceptus, Inc., Bayer HealthCare AG (Germany) is the sponsor of the trial.
Completion Date
Completion Date Type
Actual
Conditions
Contraceptive Usage
Eligibility Criteria
Inclusion Criteria:
* Women who are 21 to 44 years of age
* Women who are between 90-300 pounds (40-136 kilograms)
* Women who are scheduled to undergo an Essure micro-insert placement procedure for permanent birth control
* Women who are willing to accept the risk of pregnancy occurring while relying on the Essure device for prevention of pregnancy
* Women who are believed to have two viable fallopian tubes
* Women who are able and willing to provide written informed consent
* Women who have the mental capacity to understand the Informed Consent, comply with the protocol requirements, and provide reliable feedback regarding device wearing
* Women who can be available for all study visits
* Women who are willing to allow data to be shared with the sponsor and with regulatory bodies
* Women who are not contraindicated for the Essure procedure according to the Essure Instructions for Use (IFU)
Exclusion Criteria:
* Women who have known proximal tubal occlusion in either fallopian tube
* Women who have had a fallopian tube sterilization procedure
* Women who have a unicornuate uterus
* Women who have known endometrial or myometrial pathology that is likely to prevent access to the fallopian tube ostia
* Women who are scheduled to undergo any other intrauterine procedures at the time of Essure placement
* Women who are pregnant or suspected of being pregnant
* Women who have had a delivery or termination of pregnancy within the last six weeks
* Women who have an active or recent upper or lower pelvic infection
* Women who are contraindicated for Essure micro-insert placement according to the Essure Instructions for Use (IFU)
* Women who have a known intolerance to transvaginal imaging
* Women who are 21 to 44 years of age
* Women who are between 90-300 pounds (40-136 kilograms)
* Women who are scheduled to undergo an Essure micro-insert placement procedure for permanent birth control
* Women who are willing to accept the risk of pregnancy occurring while relying on the Essure device for prevention of pregnancy
* Women who are believed to have two viable fallopian tubes
* Women who are able and willing to provide written informed consent
* Women who have the mental capacity to understand the Informed Consent, comply with the protocol requirements, and provide reliable feedback regarding device wearing
* Women who can be available for all study visits
* Women who are willing to allow data to be shared with the sponsor and with regulatory bodies
* Women who are not contraindicated for the Essure procedure according to the Essure Instructions for Use (IFU)
Exclusion Criteria:
* Women who have known proximal tubal occlusion in either fallopian tube
* Women who have had a fallopian tube sterilization procedure
* Women who have a unicornuate uterus
* Women who have known endometrial or myometrial pathology that is likely to prevent access to the fallopian tube ostia
* Women who are scheduled to undergo any other intrauterine procedures at the time of Essure placement
* Women who are pregnant or suspected of being pregnant
* Women who have had a delivery or termination of pregnancy within the last six weeks
* Women who have an active or recent upper or lower pelvic infection
* Women who are contraindicated for Essure micro-insert placement according to the Essure Instructions for Use (IFU)
* Women who have a known intolerance to transvaginal imaging
Inclusion Criteria
Inclusion Criteria:
* Women who are 21 to 44 years of age
* Women who are between 90-300 pounds (40-136 kilograms)
* Women who are scheduled to undergo an Essure micro-insert placement procedure for permanent birth control
* Women who are willing to accept the risk of pregnancy occurring while relying on the Essure device for prevention of pregnancy
* Women who are believed to have two viable fallopian tubes
* Women who are able and willing to provide written informed consent
* Women who have the mental capacity to understand the Informed Consent, comply with the protocol requirements, and provide reliable feedback regarding device wearing
* Women who can be available for all study visits
* Women who are willing to allow data to be shared with the sponsor and with regulatory bodies
* Women who are not contraindicated for the Essure procedure according to the Essure Instructions for Use (IFU)
* Women who are 21 to 44 years of age
* Women who are between 90-300 pounds (40-136 kilograms)
* Women who are scheduled to undergo an Essure micro-insert placement procedure for permanent birth control
* Women who are willing to accept the risk of pregnancy occurring while relying on the Essure device for prevention of pregnancy
* Women who are believed to have two viable fallopian tubes
* Women who are able and willing to provide written informed consent
* Women who have the mental capacity to understand the Informed Consent, comply with the protocol requirements, and provide reliable feedback regarding device wearing
* Women who can be available for all study visits
* Women who are willing to allow data to be shared with the sponsor and with regulatory bodies
* Women who are not contraindicated for the Essure procedure according to the Essure Instructions for Use (IFU)
Gender
Female
Gender Based
false
Healthy Volunteers
No
Last Update Post Date
Last Update Post Date Type
Actual
Last Update Submit Date
Maximum Age
44 Years
Minimum Age
21 Years
NCT Id
NCT01327105
Org Class
Industry
Org Full Name
Bayer
Org Study Id
16974
Overall Status
Completed
Phases
Phase 4
Primary Completion Date
Primary Completion Date Type
Actual
Official Title
Use of Transvaginal Ultrasound to Confirm Essure® Micro-insert Placement in Women: Demonstration of Effectiveness
Primary Outcomes
Outcome Description
Rate of pregnancy at 1 and 10 years among subjects relying on Essure micro-inserts for birth control on the basis of the TVU/HSG algorithm
Outcome Measure
Effectiveness
Outcome Time Frame
Annually beginning at one year
Secondary Ids
Secondary Id
ESS-TVU
Start Date
Start Date Type
Actual
Status Verified Date
First Post Date
First Post Date Type
Estimated
First Submit Date
First Submit QC Date
Std Ages
Adult
Maximum Age Number (converted to Years and rounded down)
44
Minimum Age Number (converted to Years and rounded down)
21
Investigators
Investigator Type
Principal Investigator
Investigator Name
Mark Levie
Investigator Email
malevie@montefiore.org
Investigator Phone