Assessing Pain and Effectiveness of Carevix Device for IUD Insertions
NCT: NCT07290517 · RECRUITING
Brief Summary
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 device and tenaculum. * assess predictors of pain scores including between nulliparous and multiparous patients * assess provider-reported ease of use and satisfaction Participants (including providers) will: * be randomized to receive one device to complete the IUD procedure * complete a survey following the procedure
Frequently Asked Questions
What is Assessing Pain and Effectiveness of Carevix Device for IUD Insertions?
Assessing Pain and Effectiveness of Carevix Device for IUD Insertions is a clinical trial registered under NCT07290517. Current status: RECRUITING.
What is the status of NCT07290517?
The current status of NCT07290517 (Assessing Pain and Effectiveness of Carevix Device for IUD Insertions) is: RECRUITING.
When did Assessing Pain and Effectiveness of Carevix Device for IUD Insertions start?
Assessing Pain and Effectiveness of Carevix Device for IUD Insertions started on 2026-03-11.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.