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RecruitingNCT06952959Updated May 1, 2025

The Effects of Cosmetic Acupuncture

An interventional study of Acupuncture in Aging and Skin Health, sponsored by China Medical University Hospital. Recruiting at 1 site in Taiwan. Open to participants aged 30 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-05-01.

Sponsored by China Medical University Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Mar 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Apr 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
30 Years to 60 Years
Sex
All
01

Study summary

The study recruited 40 subjects and divided them into an intervention group and a waiting list group in a 1:1 ratio using a randomized controlled trial. The changes in skin health and aging-related indicators before and after TCM cosmetic acupuncture treatment were analyzed. The subjects are of all genders and aged between 30 and 60 years old. The TCM cosmetic acupuncture treatment is arranged twice a week for a three-week course. The study will conduct a skin test before and after the TCM cosmetic acupuncture, and use the Antera 3D smart skin detector to comprehensively evaluate the subjects' skin condition. Antera 3D Skin Detector can detect multiple skin indicators, including wrinkle depth, skin tone uniformity and subtle changes in the skin surface, melanin, red pigment, etc. After the treatment, the subjects' acceptance and satisfaction with TCM cosmetic acupuncture were collected.

02

Conditions studied

  • Aging
  • Skin Health
03

In context

Lead sponsor

China Medical University Hospital is the lead sponsor of 464 studies on the registry; 116 are open to participants now.

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

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • both female and male
  • 30 to 60 years old
  • never had acupuncture beauty treatment, or the last time they had acupuncture beauty treatment has been more than six months.

Exclusion criteria

Exclusion Criteria:

  • medical cosmetic fillers on their face
  • cosmetic surgery
  • needle sickness
  • afraid of acupuncture
  • wounds on the facial skin
  • poor wound healing
  • abnormal coagulation function
  • severe diabetes
  • keloids
  • dialysis
  • cancer patients undergoing chemotherapy or radiotherapy
  • pregnant
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Cosmetic acupuncture group

    accept treatment session

    Other: Acupuncture

  • Other
    Waitinglist for cosmetic acupuncture group

    wait for 3 weeks then accept the same treatment session

    Other: Acupuncture

Interventions

  • OtherAcupuncture

    Cosmetic acupuncture

06

What researchers measure

Primary outcomes

  1. Face Skin Texture

    Professional Intelligent Skin Analyzers accurately locate the comparison before and after cosmetic acupuncture sessions, showing high accuracy and reproducibility, analyzing Ra value (unit: µm) as arithmetic mean roughness of the skin's contours.

    Time frame: Intervention group: the 1st, 4th week; waiting list group: the 1st, 4th, and 7th week.

  2. Face Skin Color

    Professional Intelligent Skin Analyzers accurately locate the comparison before and after cosmetic acupuncture sessions, showing high accuracy and reproducibility, analyzing L\*a\*b value (no unit) as the skin's color. (L\*: Lightness, a\*: Red/Green Value, b\*: Blue/Yellow Value)

    Time frame: Intervention group: the 1st, 4th week; waiting list group: the 1st, 4th, and 7th week.

  3. Face Pore Size

    Professional Intelligent Skin Analyzers accurately locate the comparison before and after cosmetic acupuncture sessions, showing high accuracy and reproducibility, analyzing average pore volume (unit: mm²).

    Time frame: Intervention group: the 1st, 4th week; waiting list group: the 1st, 4th, and 7th week.

Secondary outcomes

  1. The Questionnaire of satisfaction and acceptance of cosmetic acupuncture

    The questionnaire include three domains: 1. Visual Analogue Scale score measures pain intensity. The VAS consists of 10 points, with two end points representing 0 ("no pain") and 10 ("pain as bad as it could possibly be"). 2. The acceptance of cosmetic acupuncture has 0\~4 points, 0 representing "unacceptable" and 4 representing "totally acceptable". 3. Facial Check Sheet(FCS) has 12 items about the satisfaction of the improvement of face appearance including wrinkles, laxity, facial shape, and pigmented spots, and so on. 0 representing "very dissatisfied" and 4 representing "very satisfied". Subjects can also choose "no need to pay attention" if they don't have the concerned problems of appearance.

    Time frame: Intervention group: the 4th week; waiting list group: the 7th week.

07

Study locations

1 of 1 sites recruiting
  • China medical university hospital
    Taichung, 40447, Taiwan
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06952959
Lead sponsor
China Medical University Hospital
Responsible party
Chia-Hui Lin (Attending Physician, China Medical University Hospital) — Principal investigator
First posted
May 1, 2025
Start date
Apr 10, 2025
Primary completion
Mar 31, 2026 (estimated)
Completion
Mar 31, 2026 (estimated)
Last update
May 1, 2025

Study contacts

Chia-Hui Lin
Contact
ffyeva@gmail.com
886+910127501

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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