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NCT07290517 · ClinicalTrials.gov registry record · NA
Assessing Pain and Effectiveness of Carevix Device for IUD Insertions
A NA study, sponsored by Indiana University.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT07290517 is a NA study that is actively recruiting participants, run by Indiana University. The registered enrollment target is 100 participants.
The verdict
NCT07290517, a NA study, is actively recruiting participants, sponsored by Indiana University.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study 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
Interventions
- DEVICE Carevix
- DEVICE Tenaculum
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2026-03-11 |
| Est. Completion | 2027-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07290517
The ClinicalTrials.gov registry entry for NCT07290517 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Carevix is the first listed.
NCT07290517 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT07290517 about?
NCT07290517 is a clinical study titled "Assessing Pain and Effectiveness of Carevix Device for IUD Insertions". 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). O...
What is the current status of trial NCT07290517?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2026-03-11. Estimated completion is 2027-03.
What interventions are being tested in trial NCT07290517?
The interventions under investigation include: Carevix (DEVICE), Tenaculum (DEVICE).
Who is sponsoring clinical trial NCT07290517?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
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