RFMN in Combination With 1927 nm Thulium Laser for Treating Photoaged Skin

Sponsor
Universitätsklinikum Hamburg-Eppendorf (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06029725
Collaborator
(none)
35
1
2
16.5
2.1

Study Details

Study Description

Brief Summary

The appearance of the aging skin is influenced by different factors including by the reduced elasticity and increased laxity of the skin, the decreasing volume as well as pigmentation disorders and dilated vascular markings. Currently, there are different methods available to treat the aging skin. Here, the combined treatment of radiofrequency micro needling (RFMN) and thulium laser has been commonly used in clinical practice.

The aim of this clinical study is to investigate the efficacy, patient satisfaction, safety of RFMN and thulium laser treatment in patients with facial, age-related skin laxity, wrinkles, and pigmented lesions.

Condition or Disease Intervention/Treatment Phase
  • Device: radiofrequency microneedling combined with 1927 nm thulium laser
  • Device: radiofrequency microneedling monotherapy
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
35 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
RFMN in Combination With 1927 nm Thulium Laser for Treating Photoaged Skin: a Prospective, Controlled Study
Anticipated Study Start Date :
Oct 15, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Mar 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: RFMN+Thulium

Device: radiofrequency microneedling combined with 1927 nm thulium laser
session: radiofrequency microneedling + 1927 nm thulium laser session: 1927 nm thulium laser monotherapy session: 1927 nm thulium laser monotherapy

Active Comparator: RFMN

Device: radiofrequency microneedling monotherapy
1 session: radiofrequency microneedling monotherapy

Outcome Measures

Primary Outcome Measures

  1. Change in wrinkles [6 months after last treatment session]

    software-assisted evaluation of wrinkles (Vectra(R) Software, Canfield)

  2. Change in volume [6 months after last treatment session]

    software-assisted evaluation of volume (Vectra(R) Software, Canfield)

  3. Change in pigmentation [6 months after last treatment session]

    software-assisted evaluation of pigmentation (Vectra(R) Software, Canfield)

Secondary Outcome Measures

  1. Pain intensity [10 minutes after starting each treatment session, one treatment session takes 30-50 minutes]

    pain intensity (numeric rating scale) during treatment

  2. Adverse Events [before every treatment session, at every follow-up visit (3 and 6 months post-treatment)]

    number of adverse events (AE)

  3. Withdrawals due to AE [before every treatment session, at every follow-up visit (3 and 6 months post-treatment)]

    number of withdrawal due to AE

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Men and women from the age of 30 years

  • good general condition, no relevant previous diseases

  • Presence of wrinkles, dermatochalasis on the face, pigment spots, which are an indication for RFMN and thulium laser or comparable methods

  • Cognitive ability and willingness to give consent (informed consent)

  • Be willing and able to attend follow-up visits

Exclusion Criteria:
  • Age < 30 years

  • Pregnancy or breastfeeding

  • Excessive subcutaneous fatty tissue under the cheeks

  • Significant scarring of the region to be treated

  • open wounds or lesions of the region to be treated

  • Severe or cystic facial acne

  • Metallic implants in the face or neck region

  • Mental illnesses (psychoses, body perception disorders)

  • Use of isotretinoin or other retinoids, psychotropic drugs, coumarins or heparins in the last 2 weeks

  • Fillers in the region to be treated < 4 weeks prior and during the study period

  • Resurfacing (fractional, ablative, nonablative) of the region of interest < 2 months prior and during the study period

  • Plastic aesthetic procedures or other surgical procedures < 6 months prior and during the study period

  • Tendency to have excessive scarring

  • Lack of informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Medical Center Hamburg-Eppendorf Hamburg Germany 20251

Sponsors and Collaborators

  • Universitätsklinikum Hamburg-Eppendorf

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Lynhda Nguyen, Principle Investigator, Universitätsklinikum Hamburg-Eppendorf
ClinicalTrials.gov Identifier:
NCT06029725
Other Study ID Numbers:
  • 03-23
First Posted:
Sep 8, 2023
Last Update Posted:
Sep 15, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Sep 15, 2023