Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT07031206 · ClinicalTrials.gov registry record · Phase 2
Investigating Pre-Procedural Anxiety and Effect of Analgesia on Intrauterine Device Placement and Endometrial Biopsy
A Phase 2 study, sponsored by The University of Texas Health Science Center, Houston.
- Not yet
- Registry status
- Phase 2
- Development phase
- 152
- Enrollment target
NCT07031206 is a Phase 2 study that has not yet begun recruiting, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 152 participants.
The verdict
NCT07031206, a Phase 2 study, has not yet begun recruiting, sponsored by The University of Texas Health Science Center, Houston.
- NOT YET RECRUITING
- Registry status
- Phase 2
- Development phase
- 152 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate pre-procedural anxiety and patient pain perception with IUD insertion/ EMB procedure when using analgesia versus no analgesia by the end of the study and to evaluate the effect of age, race, parity, type of IUD and anxiety on pain and to offer better pain management in our patient population, undergoing IUD insertion/EMB procedure at the end of our study.
Interventions
- DRUG Paracervical block- Lidocaine without epinephrine
- DRUG Benzocaine Gel applied to the cervix
- DRUG Hydroxyzine Hydrochloride
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 152 participants |
| Start Date | 2025-07-01 |
| Est. Completion | 2026-05-05 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07031206
The ClinicalTrials.gov registry entry for NCT07031206 describes a study currently listed as not yet recruiting, categorized as Phase 2. The registered enrollment target is 152 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 Paracervical block- Lidocaine without epinephrine is the first listed.
NCT07031206 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT07031206 about?
NCT07031206 is a clinical study titled "Investigating Pre-Procedural Anxiety and Effect of Analgesia on Intrauterine Device Placement and Endometrial Biopsy". The purpose of this study is to evaluate pre-procedural anxiety and patient pain perception with IUD insertion/ EMB procedure when using analgesia versus no analgesia by the end of the study and to evaluate the effect of age, race, parity, type of IUD and anxiety on pain and to offer better pain man...
What is the current status of trial NCT07031206?
This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 152 participants. The study started on 2025-07-01. Estimated completion is 2026-05-05.
What interventions are being tested in trial NCT07031206?
The interventions under investigation include: Paracervical block- Lidocaine without epinephrine (DRUG), Benzocaine Gel applied to the cervix (DRUG), Hydroxyzine Hydrochloride (DRUG).
Who is sponsoring clinical trial NCT07031206?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.