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CompletedNCT07877870Updated Oct 16, 2026

Tissue Repositioning Versus Tissue Support in Thread Lifting for Nasolabial Fold Correction: A Randomized, Evaluator-Blinded, Parallel-Group Controlled Trial

An interventional study of predominantly tissue-repositioning thread lifting and predominantly tissue-support thread-lifting in Nasolabial Fold, sponsored by Beijing Tsinghua Chang Gung Hospital. Completed at 1 site in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by Beijing Tsinghua Chang Gung Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 years 3 months after the study started (first participant enrolled Jun 2022, registered Oct 2026).
Updated Oct 16, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
182
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This randomized clinical trial compares two minimally invasive thread-lifting procedures for improving moderate-to-severe nasolabial folds, the lines that run from the sides of the nose toward the corners of the mouth. Both procedures use absorbable threads placed under the skin, but they differ in their main treatment approach. One procedure is designed primarily to lift and reposition sagging facial tissues, whereas the other is designed primarily to provide local support and added volume beneath and around the folds.

Approximately 180 adults with moderate-to-severe nasolabial folds will be randomly assigned to one of the two treatment groups. An independent evaluator who does not know the treatment assignment will assess changes in the nasolabial folds during follow-up. The main purpose of the study is to compare the effectiveness of the two procedures 7 months after treatment. The study will also assess early improvement, participants' and evaluators' overall impressions of the results, and treatment-related adverse events and safety.

02

Conditions studied

  • Nasolabial Fold

Keywords

  • Nasolabial fold; thread lifting; polydioxanone; facial rejuvenation; randomized controlled trial
03

In context

Lead sponsor

Beijing Tsinghua Chang Gung Hospital is the lead sponsor of 102 studies on the registry; 52 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Healthy Chinese female or male between 18 and 65 years.

    • Bilateral nasolabial fold wrinkles assessed as severity grade ≥ 3 on the Wrinkle Severity Rating Scale (WSRS).
    • Willing to accept thread lifting for nasolabial fold correction.
    • The subject voluntarily participates in this trial and has signed the informed consent.

Exclusion criteria

Exclusion Criteria:

  • ·With a hypersensitive constitution.

    • With tendency to develop hypertrophic or keloid scars.
    • With known history of bleeding disorders.
    • With inflammation or infectious cutaneous disorders in or near the studied zones (herpes, acne, mycosis, papilloma, …).
    • With psychological disorders or psychiatric illnesses.
    • Under laser therapy or chemical peeling in the treatment area within 6 months, or injection of botulinum toxin type A within 6 months.
    • Injection of non-permanent fillers (e.g., hyaluronic acid, collagen) in the treatment area within 1 year.
    • Prior facial implantation of permanent fillers.
    • Use of anticoagulant or antiplatelet medications within 2 weeks prior to surgery.
    • Women who were pregnant, planning pregnancy, or breastfeeding.
    • Other conditions deemed unsuitable for participation in the clinical trial by the investigator.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
182 participants (actual)

Study arms

  • Experimental
    Experimental

    Participants received a predominantly tissue-repositioning and multi-plane tissue-lifting thread-lifting protocol for correction of moderate-to-severe nasolabial folds.

    Procedure: predominantly tissue-repositioning thread lifting

  • Active comparator
    Active Comparator

    A predominantly tissue-support and multiregional volumization thread-lifting protocol for correction of moderate-to-severe nasolabial folds.

    Procedure: predominantly tissue-support thread-lifting

Interventions

  • Procedurepredominantly tissue-repositioning thread lifting

    A predominantly tissue-repositioning and multi-plane tissue-lifting thread-lifting protocol for correction of moderate-to-severe nasolabial folds.

  • Procedurepredominantly tissue-support thread-lifting

    A predominantly tissue-support and multiregional volumization thread-lifting protocol for correction of moderate-to-severe nasolabial folds.

06

What researchers measure

Primary outcomes

  1. WSRS effective rate (ER) for NLF correction at 7 months post-operation

    The ER was calculated as the percentage of effective responses among subjects in the relevant analysis population.

    Time frame: 7 months post-operation

Secondary outcomes

  1. ERs of NLF correction

    The ERs of NLF correction immediately after surgery (V2) and at 14 days (V3), 1 month (V4), and 3 months (V5) postoperatively.

    Time frame: Immediately after surgery (V2) and at 14 days (V3), 1 month (V4), and 3 months (V5) postoperatively

  2. Percentage improvement in WSRS scores

    Percentage improvement in WSRS scores (%) was calculated as \[(baseline WSRS score - post-operation WSRS score) / baseline WSRS score\] × 100%

    Time frame: Immediately after surgery (V2), and at 14 days (V3), 1 month (V4), 3 months (V5), and 7 months (V6) postoperatively.

  3. The mean GAIS scores

    The mean GAIS scores at all follow-up visits (V2-V6). The GAIS was a 5-point scale (1 = very much improved; 5 = worse), assessed independently by the subjects and independent evaluators.

    Time frame: Immediately after surgery (V2), and at 14 days (V3), 1 month (V4), 3 months (V5), and 7 months (V6) postoperatively.

07

Study locations

1 site
  • Beijing Tsinghua Changgung Hospital
    Beijing, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jun 2022 to primary completion in Nov 2023, 16 months.

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

Registered
Oct 11, 2026
First posted
Oct 16, 2026
StartActual
Jun 21, 2022
Primary completionActual
Nov 3, 2023
CompletionActual
Nov 20, 2023
Last update
Oct 16, 2026
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.
Registered
First appeared on the registry. No changes since
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07877870
Responsible party
Sponsor
First posted
Oct 16, 2026
Start date
Jun 21, 2022
Primary completion
Nov 3, 2023
Completion
Nov 20, 2023
Last update
Oct 16, 2026

Study contacts

Leiyue Li, Ph.D.
study director · Math, Computer Science, and Statistics Department, St. Lawrence University

Oversight

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

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This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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