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ACTIVE NOT RECRUITING NA

Clinical Study to Evaluate the Safety and Efficacy of Candela Technology

NCT06202274 · View on ClinicalTrials.gov ↗

Study Summary

This is a non-randomized, multi-center, open-label, prospective clinical study evaluating the clinical treatment with Candela Medical Technology.

Interventions

  • DEVICE Nordlys, Gentle, Picoway, Vbeam, Profound, Profound Matrix, eTwo, Exceed, CO2RE

Study Locations (3)

Florida

  • Center for Morden Aesthetic Medicine — Jacksonville

Massachusetts

  • Candela Institue for Excellence — Marlborough

Other

  • Yokneam Candela Clinic — Yokneam Illit

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2023-10-04
Est. Completion 2029-10-04
Phase NA

Sponsor

Candela Corporation

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06202274

The ClinicalTrials.gov registry entry for NCT06202274 describes a study currently listed as active not recruiting. It is categorized as NA, 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 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Candela Corporation, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Acne appearing as the primary indexed condition, and to 1 intervention — of which Nordlys, Gentle, Picoway, Vbeam, Profound, Profound Matrix, eTwo, Exceed, CO2RE 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: NCT06202274 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Florida, Massachusetts, Other. 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 NCT06202274 about?

NCT06202274 is a clinical study titled "Clinical Study to Evaluate the Safety and Efficacy of Candela Technology". This is a non-randomized, multi-center, open-label, prospective clinical study evaluating the clinical treatment with Candela Medical Technology.

What is the current status of trial NCT06202274?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 500 participants. The study started on 2023-10-04. Estimated completion is 2029-10-04.

What conditions does trial NCT06202274 study?

This clinical trial studies the following conditions: Acne, Wrinkle, Scars, Tattoo Removal, Skin Conditions. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06202274?

The interventions under investigation include: Nordlys, Gentle, Picoway, Vbeam, Profound, Profound Matrix, eTwo, Exceed, CO2RE (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06202274?

This trial is sponsored by Candela Corporation, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06202274 being conducted?

This trial has 3 study locations across Florida, Massachusetts. 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