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Comparing Polydioxanone Thread Embedding Acupuncture and Manual Acupuncture for Nasolabial Fold Reduction

U

University of Indonesia (UI)

Status

Completed

Conditions

Aging Problems
Wrinkle

Treatments

Other: Manual acupuncture
Other: Thread embedding acupuncture

Study type

Interventional

Funder types

Other

Identifiers

NCT05098912
21060651

Details and patient eligibility

About

This study was aimed to compare the effectiveness of polydioxanone thread embedding acupuncture and manual acupuncture on the reduction of the nasolabial fold. One cycle of therapy in the manual acupuncture group (MA) was carried out with 6 sessions of manual acupuncture therapy while one cycle of therapy in the thread embedding acupuncture group (TEA) received 1 single session of thread embedding acupuncture. The outcome of the study was assessed based on the length of the nasolabial fold as measured by a digital vernier caliper, changes in wrinkle severity rating scale, and patient's subjective opinion of her nasolabial fold using visual analog scale. Outcome measurements were carried out after completing 1 cycle, and follow up at 2 weeks, 1 month, 2 months and 3 months after completing 1 cycle.

Enrollment

30 patients

Sex

Female

Ages

30 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Woman
  • Age 30-50 years old
  • WSRS scale 3 to 4
  • Willing to follow the research to completion
  • Subjects who do not have a history of filler injection and/implants, laser therapy, microdermabrasion, peeling, botulinum toxin therapy, manual acupuncture on the face, thread embedding acupuncture on the face and does not either oral or topically use collagen within 6 months
  • Body mass index of ≥ 18.5
  • Signed the informed consent

Exclusion criteria

  • Subjects with facial muscle paralysis disorders
  • Subjects with history of keloids and/or hypertrophic scars, subjects with tumors or infection or inflammation at the treatment area
  • Subjects with allergies to stainless steel, PDO threads, topical anesthetics lidocaine
  • Pregnant and lactating subjects
  • Subjects with cancer
  • Subjects with history of bleeding disorders or are taking anticoagulant or antiplatelet.
  • Subjects suffering from fever (≥ 37.5°C), cough, fatigue
  • Subjects with blood glucose POCT (Point of Care Testing) levels of ≥ 200 mg/dl

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Manual acupuncture
Active Comparator group
Description:
The subjects/population of this study is woman at age 30-50 who meet the inclusion criteria. Subjects group with manual acupuncture treatment will be treated with 6 session of manual acupuncture at: From the superior of zygomatic arch through ST 2 to LI 20 bilaterally using a needle size of 0.25 x 60 mm From the inferior of zygomatic arch through SI 18 to ST 4 bilaterally using a needle size of 0.25 x 60 mm From ST 7 to ST 4 bilaterally using a needle size of 0.25 x 60 mm Along the nasolabial crease through ST 4 to the bilateral EXHN-8 using a needle size of 0.25 x 40 mm
Treatment:
Other: Manual acupuncture
Thread embedding acupuncture
Active Comparator group
Description:
The subjects/population of this study is woman at age 30-50 who meet the inclusion criteria. Subjects group with thread embedding acupuncture group treatment will be treated with 1 session of thread embedding acupuncture at: From the superior of zygomatic arch through ST 2 to LI 20 bilaterally using a gauge and length of the needle of 31G x 50 mm From the inferior of zygomatic arch through SI 18 to ST 4 bilaterally using a gauge and length of the needle of 31G x 50 mm From ST 7 to ST 4 bilaterally using a gauge and length of the needle of 31G x 50 mm Along the nasolabial crease through ST 4 to the bilateral EXHN-8 using a gauge and length of the needle of 31G x 30 mm
Treatment:
Other: Thread embedding acupuncture

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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