Improvement of Symptoms After Removal of the Essure® Contraceptive Implant
Recruiting
N/A
Interventional Study
Implant Complication
Contraceptive Device; Complications
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 35 – 75
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 444 (estimated)
- Sponsor
- Hospices Civils de Lyon · Other
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About This Trial
ESSURE® is an implantable medical device for definitive and irreversible sterilization indicated for adult women of childbearing age. These implants are inserted into the fallopian tubes by hysteroscopy. Marketed in 2002, ESSURE® contraceptive implants were withdrawn from the French market in 2017 (and worldwide in 2017 and 2018) following the observation in certain patients of polymorphic and non…
Trial Locations
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Eligibility Criteria
* Inclusion Criteria \* :
ESSURE Group:
* woman aged 35 to 75
* patient with at least one Essure® implant
* surgical intervention planned because the patient is symptomatic: removal of the Essure® implant(s)
* planned intervention via vaginal route, laparoscopy, robotic surgery, or Transvaginal na…
Contacts