Skip to main content
OpenTrials
Completed

NCT Number: NCT04362891

Four Hyaluronic Acid Fillers for Lip Augmentation

There is need for evidence-based and reproducible data comparing the safety, longevity and patient satisfaction propensity of the various HA soft tissue filler products. Among cosmetic HA soft tissue filler procedures, especially the lip augmentation has become common. Therefore, the aim of this study is to determine whether a statistically significant difference can be detected in the safety, longevity and/or patient satisfaction related to four HA soft tissue filler products widely used for cosmetic lip augmentation. Specifically, the aim of this study is to determine whether superiority of one or more product(s) over the others can be detected.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Faceland Almere, Almere Stad, Flevoland, Netherlands

Loading trial locations.

About this study

Rationale: Currently, hyaluronic acid (HA) soft tissue fillers are widely employed in cosmetic medical practice for facial contouring and rejuvenation. Among these procedures, especially the lip augmentation has become common. To this end various products have become commercially available, however to date no robust evidence is available to support the safety, longevity or patient satisfaction propensity superiority of one product over the others.

Objective: To assess whether superiority in safety, longevity and patient satisfaction propensity can be shown of one of four most frequently used FDA-approved and/or CE marked HA fillers worldwide, used to augment the lip, over the others.

Study design: Multi-center, randomized, controlled, four group, parallel, triple-blind clinical trial of 160 adult participants.

Study population: Consecutive healthy individuals with no history of previous lip treatment and a self-reported wish for lip augmentation, who present at one of the private cosmetic medicine clinics in the Netherlands, will be recruited.

Intervention (if applicable): After giving informed consent, participants will be randomized to receive a protocoled lip augmentation procedure by the injection of either 1 mL of brand A, B, C or D.

Main study parameters/endpoints: The primary outcome measure will be the absolute lip volume augmentation as measured by the Lemperle Lip Index from baseline to 3-months follow-up. Secondary outcomes will include the incidence of serious adverse reactions and side effects related to the procedure, the absolute volume augmentation from baseline to 2-weeks follow-up and self-reported quality of life and satisfaction with aesthetic results from baseline to 2-weeks follow-up as measured by validated FACE-Q questionnaire scores.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years or over.
  • Female sex.
  • No history of previous lip augmentation treatment.
  • Oral and written informed consent to participate in the study.
  • Desire for cosmetic lip augmentation to improve one's physical or mental well-being.
  • Actively treatment seeking (patient actively chooses to make an appointment at a Faceland private cosmetic clinic without invitation).
  • Small to moderately full lip volume (Merz Lip Scale score 0 - 2 out of 4).

Exclusion criteria

  • Active peri-oral infection in vicinity of injection site
  • Tumour in vicinity of injection site
  • Active tuberculosis
  • Pregnant or breast-feeding
  • History of severe hypersensitivity to filler components (sodium hyaluronate preparations or local anesthetics of the -amide type, gram-positive proteins, wasps/bees or the hyaluronidase enzyme)
  • Active collagenosis (e.g., active systemic lupus)
  • Graft vs. host disease
  • Active Hashimoto's disease
  • Use of thrombolytics or anticoagulants with high bleeding risk
  • General infection
  • Porphyria
  • Untreated epilepsy
  • Keloid tendency
  • Cardiac arrythmia
  • Severe liver or kidney disease
  • Fulfilling the DSM-5 diagnostic criteria for Body Dyspmorphic Disorder
  • Concurrent laser- peeling- or dermabrasia treatment

Treatment and study plan

Cosmetic lip augmentation

Procedure

The primary study treatment site will be the vermilion (body of the lip); additional areas (vermilion borders, Cupid's bow, philtral columns, and/or oral commissures) will be treated if deemed appropriate by the treating physician. Treatment will be administered through intradermal, subdermal, and/or intramuscular injection within the orbicularis oris muscle. Injection techniques for each area will include linear threading, serial puncture, fanning, and/or cross-hatching. The treating physician will determine the appropriate volume to inject based on clinical experience and the subject's goals for lip augmentation.

Primary outcomes

  1. Longevity of absolute lip volume augmentation

    Time frame: from baseline to 3-months follow-up

    The primary outcome will be the longevity of the absolute lip volume augmentation, as measured by the modified Lemperle Lip Index (vertical height in mm).

Secondary outcomes

  1. Patient satisfaction (lip appraisal)

    Time frame: from baseline to 3-months follow-up

    Patient satisfaction with the treatment as measured by validated FACE-Q questionnaire "Lips" score.

  2. Quality of Life (Social)

    Time frame: baseline to 3-months follow-up

    Quality of Life as measured by validated FACE-Q questionnaire "Social Function" score.

  3. Quality of Life (Psychological)

    Time frame: baseline to 3-months follow-up

    Quality of Life as measured by validated FACE-Q questionnaire "Psychological Wellbeing" score.

  4. Product safety (serious adverse events)

    Time frame: baseline, 2-weeks and 3-months follow-up

    Product safety, as measured by serious adverse events related to the procedure.

Other outcomes

  1. Effectiveness of absolute lip volume augmentation at week 2

    Time frame: from baseline to 2-weeks follow-up

    A between-group difference in volume augmentation from baseline to 2-weeks follow-up,

  2. Patient satisfaction (with treatment outcome)

    Time frame: at 2 weeks and 3 months follow-up

    Patient satisfaction with the treatment as measured by validated FACE-Q questionnaire scores "Satisfaction with Outcome of Treatment" score.

  3. Patient satisfaction (with decision)

    Time frame: at 2 weeks and 3 months follow-up

    Patient satisfaction with the treatment as measured by validated FACE-Q questionnaire "Satisfaction with Decision to Have Treatment" score.

  4. Side-effects (psychological impact of recovery from treatment)

    Time frame: at 2 weeks and 3 months follow-up

    Side-effects, as measured by the FACE-Q questionnaire "Early Life Impact" score.

  5. Side-effects (physical discomfort)

    Time frame: baseline, 2-weeks and 3-months follow-up

    Side-effects, as measured by the FACE-Q questionnaire "Adverse Effects Lips" score.

  6. Side-effects (recovery of side-effects)

    Time frame: baseline, 2-weeks and 3-months follow-up

    Side-effects, as measured by validated FACE-Q questionnaire scores "Recovery Early Symptoms" score.

  7. Absolute lip volume augmentation at week 2

    Time frame: from baseline to 2-weeks follow-up

    The absolute lip volume augmentation as measured by the Lemperle Lip Index.

Sponsors and collaborators

Lead sponsor

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Other

Collaborators

  • Faceland Clinics

Registry information

Official study title

Safety, Longevity and Patient Satisfaction Comparison of Four Hyaluronic Acid Soft Tissue Fillers in Lip Augmentation: Study Protocol for a Randomized Controlled Clinical Trial

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Apr 27, 2020
Registry last updated
Mar 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.