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RECRUITING Phase 4

Comparison of Compounded Topical Anesthetics

NCT06569537 · View on ClinicalTrials.gov ↗

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

FieldValue
Enrollment Target 64 participants
Start Date 2024-10-22
Est. Completion 2026-01
Phase Phase 4

Sponsor

Dartmouth-Hitchcock Medical Center

396 total trials

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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. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dartmouth-Hitchcock Medical Center, which has 396 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06569537 reports 1 study location spanning 1 distinct geographic area — top geographies include New Hampshire. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06569537?

The interventions under investigation include: Lidocaine topical (DRUG), BLT (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06569537?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 396 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial