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NCT02904915 · ClinicalTrials.gov registry record · Phase 4
Paracervical Block Versus No Paracervical Block During IUD Insertion
A Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- Phase 4
- Development phase
- 50
- Enrollment target
NCT02904915 is a Phase 4 study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 50 participants.
The verdict
NCT02904915, a Phase 4 study, has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the pain level and level of discomfort with paracervical block versus no analgesia in women who present to the University of Texas (UT) Physicians Obstetrics and Gynecology Continuity Clinic, The UT Physicians Women's Center, and the UT Physicians Women's Center- Bellaire for IUD insertion.
Interventions
- DRUG Lidocaine
- OTHER No analgesia
- DEVICE Intrauterine device (IUD)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2017-01-12 |
| Est. Completion | 2017-10-09 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02904915
The ClinicalTrials.gov registry entry for NCT02904915 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Lidocaine is the first listed.
NCT02904915 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02904915 about?
NCT02904915 is a clinical study titled "Paracervical Block Versus No Paracervical Block During IUD Insertion". The purpose of this study is to compare the pain level and level of discomfort with paracervical block versus no analgesia in women who present to the University of Texas (UT) Physicians Obstetrics and Gynecology Continuity Clinic, The UT Physicians Women's Center, and the UT Physicians Women's Cent...
What is the current status of trial NCT02904915?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2017-01-12. Estimated completion is 2017-10-09.
What interventions are being tested in trial NCT02904915?
The interventions under investigation include: Lidocaine (DRUG), No analgesia (OTHER), Intrauterine device (IUD) (DEVICE).
Who is sponsoring clinical trial NCT02904915?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
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