Assessing Pain and Effectiveness of Carevix Device for IUD Insertions
Recruiting
N/A
Interventional Study
IUD
Abnormal Uterine Bleeding
Pain, Cervical
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 100 (estimated)
- Sponsor
- Indiana University · Other
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About This Trial
The goal of this clinical trial is to evaluate patient-reported pain, bleeding, and device efficiency along with provider satisfaction and ease of use between IUD insertions using a suction cervical stabilizer (new device, FDA approved, atraumatic) and single-tooth tenaculum (standard, traumatic). Our aims are to:
* assess and compare patient-reported pain during IUD insertion between the Carevix…
Trial Locations
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Eligibility Criteria
Inclusion Criteria (to be assessed prior to procedure):
* Age 18 years or older
* Able to consent on their own
* Scheduled and will undergo an IUD insertion within 90 days of consent
* Planned use of cervical stabilization device for placement
* Procedure being performed by a trained provider
* Pro…
Contacts