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NCT06569537 · ClinicalTrials.gov registry record · Phase 4
Comparison of Compounded Topical Anesthetics
A Phase 4 study of Procedural Pain, sponsored by Dartmouth-Hitchcock Medical Center.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 64
- Enrollment target
- 1
- Study location
NCT06569537 is a Phase 4 study of Procedural Pain that is actively recruiting participants, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 64 participants, above the 54-participant average among 9 other Procedural Pain trials with a reported enrollment target (19% higher). The trial reports 1 study location across 1 state.
The verdict
NCT06569537, a Phase 4 study of Procedural Pain, is actively recruiting participants, sponsored by Dartmouth-Hitchcock Medical Center.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 64 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective for this pilot study is to evaluate the efficacy of the compounded topical anesthetic Benzocaine 20%/ Lidocaine 8%/Tetracaine 4% (BLT) compared to 4% Lidocaine topical in providing relief of pain during IPL, PDL, and microneedling procedures.
Conditions Studied
Interventions
- DRUG Lidocaine topical
- DRUG BLT
Study Locations (1)
New Hampshire
- Dartmouth Hitchcock Dermatology Clinic - Lebanon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2024-10-22 |
| Est. Completion | 2026-01 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06569537
The ClinicalTrials.gov registry entry for NCT06569537 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 54-participant average among 9 other Procedural Pain trials with a reported enrollment target (19% higher). The listed sponsor is Dartmouth-Hitchcock Medical Center, which has 427 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Procedural Pain appearing as the primary indexed condition, and to 2 interventions - of which Lidocaine topical is the first listed.
NCT06569537 reports 1 study location spanning 1 distinct geographic area - top geographies include New Hampshire.
Frequently Asked Questions
What is clinical trial NCT06569537 about?
NCT06569537 is a clinical study titled "Comparison of Compounded Topical Anesthetics". The primary objective for this pilot study is to evaluate the efficacy of the compounded topical anesthetic Benzocaine 20%/ Lidocaine 8%/Tetracaine 4% (BLT) compared to 4% Lidocaine topical in providing relief of pain during IPL, PDL, and microneedling procedures.
What is the current status of trial NCT06569537?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 64 participants. The study started on 2024-10-22. Estimated completion is 2026-01.
What conditions does trial NCT06569537 study?
This clinical trial studies the following conditions: Procedural Pain.
What interventions are being tested in trial NCT06569537?
The interventions under investigation include: Lidocaine topical (DRUG), BLT (DRUG).
Who is sponsoring clinical trial NCT06569537?
This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06569537 being conducted?
This trial has 1 study location across New Hampshire. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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