ClinicalTrials.gg
CompletedNCT03424161Updated Sep 15, 2023Results posted

Multi-Center, Clinical Evaluation of the Cutera Secret RF Device

An interventional study of Secret RF in Skin Quality, sponsored by Cutera Inc.. Completed at 1 site in United States. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-09-15.

Sponsored by Cutera Inc. · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
27
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The objectives of this study are to evaluate the efficacy and safety of the Cutera Secret RF device.

Read the detailed description

This is a multi-center, study in approximately 40 subjects, ages 18 and older. Subjects will receive treatments and will be followed at 4 and 12 weeks post the final treatment.

02

Conditions studied

  • Skin Quality
03

In context

Lead sponsor

Cutera Inc. is the lead sponsor of 42 studies on the registry; none are open to participants now.

Of its 19 completed or terminated interventional studies of FDA-regulated products, 19 (100%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Subject must be able to read, understand and sign the Form.
  2. Female or Male, age 18 and older
  3. Willing to undergo treatments with Secret RF.
  4. Willing to have very limited sun exposure and use sunscreen on the treatment area every day for the duration of the study, including the follow-up period.
  5. Subject must adhere to the follow-up schedule and study instructions.
  6. Agree to not undergo any other cosmetic procedure(s) or treatment(s) on the treatment area during the study and has no intention of having such procedures performed during the course of the study.
  7. Willing to have digital photographs taken of the treatment area and agree to use of photographs for presentation, (educational and/or marketing), publications, and any additional marketing purposes.
  8. For female subjects: not pregnant or lactating and is either , surgically sterilized, or using a medically acceptable form of prior to enrollment and during the entire course of the study.

Exclusion criteria

Exclusion Criteria:

  1. Participation in a clinical trial of another device or drug within 1 month of study participation, or during the study period.
  2. History of clotting disorders and/or current use of blood thinning medications.
  3. History of disorders or diabetes.
  4. Cardiac pacemaker or active implantable metal device in the treatment area.
  5. Allergies to metals i.e. gold.
  6. Has a history of squamous cell carcinoma or melanoma in the treatment area.
  7. Significant uncontrolled concurrent illness that in the opinion of the Investigator would make the subject unsuitable for inclusion.
  8. History of any disease or condition that could impair wound healing.
  9. History of keloid formation or abnormal/delayed wound healing.
  10. History of disease stimulated by heat, such as recurrent herpes simplex and/or herpes zoster (shingles) in the treatment area, unless treatment is conducted following a prophylactic regimen.
  11. Use of topical agents one week prior to treatment that may cause facial sensitivity.
  12. Suffering from significant skin conditions in the treated areas or inflammatory skin conditions, including but not limited to, open lacerations or abrasions, hidradenitis, rash, infection , or dermatitis of the treatment area prior to treatment (duration of resolution as per the Investigator's discretion).
  13. As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study or a condition that would compromise the subject's ability to comply with the study requirements.
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
27 participants (actual)

Study arms

  • Other
    Secret RF

    Treatment with Secret RF for skin quality

    Device: Secret RF

Interventions

  • DeviceSecret RF

    Subjects will receive treatment with the Secret RF device

06

What researchers measure

Primary outcomes

  1. Overall Aesthetic Improvement

    Efficacy of treatment(s) with Cutera Secret RF measuring the global skin improvement at the 4 week follow-up visit, and at the 12 week follow-up visit as assessed by the study investigator using GAIS: Global Aesthetic Improvement Scale (+4=Very Significant Improvement, +3=Significant Improvement, +2=Moderate Improvement, +1=Mild Improvement, or 0=No Change Higher scores indicate better outcomes

    Time frame: at 4 weeks follow-up and 12 weeks follow-up

07

Results

Posted Sep 15, 2023

Participant flow

Participant flow — Overall Study
MilestoneSecret RF
Started27
Completed10
Not completed17

Outcome measures

PrimaryOverall Aesthetic Improvement

Efficacy of treatment(s) with Cutera Secret RF measuring the global skin improvement at the 4 week follow-up visit, and at the 12 week follow-up visit as assessed by the study investigator using GAIS: Global Aesthetic Improvement Scale (+4=Very Significant Improvement, +3=Significant Improvement, +2=Moderate Improvement, +1=Mild Improvement, or 0=No Change Higher scores indicate better outcomes

Time frame:
at 4 weeks follow-up and 12 weeks follow-up
Reported as:
Mean · score on a scale
Overall Aesthetic Improvement
score on a scaleSecret RF
GAIS at the 4 week follow up1.63 ± 0.92
GAIS at the 12 week follow up2 ± 0.71

Adverse events

Collected over 12 weeks post final treatment, up to 8 months. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Secret RF0/27 (0%)0/27 (0%)27/27 (100%)
Most frequent other events
Most frequent other events
EventSecret RF
EdemaSkin and subcutaneous tissue disorders27/27
ErythemaSkin and subcutaneous tissue disorders27/27
PainSkin and subcutaneous tissue disorders20/27

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Secret RF
<=18 years0
Between 18 and 65 years26
>=65 years1
Sex: Female, Male
Sex: Female, Male(Participants)Secret RF
Female22
Male5
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Secret RF
American Indian or Alaska Native0
Asian9
Native Hawaiian or Other Pacific Islander0
Black or African American1
White17
More than one race0
Unknown or Not Reported0
08

Study locations

1 site
  • Cutera Research Center
    Brisbane, California 94005, United States
09

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2018 to primary completion in Oct 2018, 8 months.

Results were first posted in Sep 2023, 4 years 11 months after primary completion.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 25, 2018
First posted
Feb 6, 2018
StartActual
Jan 10, 2018
Primary completionActual
Oct 8, 2018
CompletionActual
Oct 8, 2018
Results first posted
Sep 15, 2023
Last update
Sep 15, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 15, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03424161
Lead sponsor
Cutera Inc.
Responsible party
Sponsor
First posted
Feb 6, 2018
Start date
Jan 10, 2018
Primary completion
Oct 8, 2018
Completion
Oct 8, 2018
Results posted
Sep 15, 2023
Last update
Sep 15, 2023

Study contacts

Stephen Ronan, MD
principal investigator · Cutera Research Center

Oversight

FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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