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Completed

NCT Number: NCT01014871

Comparison of Two Botulinum Toxins Type A on Forehead Wrinkles

Single-centre, controlled, randomized, evaluator-blinded, bilateral (split-face) comparison study in subjects with moderate to severe forehead wrinkles.

One botulinum toxin type A will be injected in one side of the forehead and the other one will be injected in the other side of the forehead at baseline. Allocation of each BoNT-A to each side of the forehead will be randomized.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

La Charité Hospital

Berlin, Germany

About this study

There are two formulations of BoNT-A available: Botox®/Vistabel®, Allergan and Dysport®/Azzalure®, Ipsen - Galderma. These formulations behave distinctly in different ways electrophysiologically and clinically and results obtained with one formulation cannot be extrapolated to the other. There are only few clinical research directly comparing the two formulations in the treatment of forehead lines.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Female Subjects of any race, from 18 to 65 years old
  • Moderate to severe horizontal forehead wrinkles at maximum contraction (2-3 on the Forehead Wrinkles Severity Scale) on both sides of the forehead
  • Negative urine pregnancy test at the Baseline visit for Subjects of childbearing potential

Exclusion criteria

  • Subjects with a washout period for procedure(s)/treatment(s) on the forehead less than:
  • Retinoid, microdermabrasion, or prescription level glycolic acid treatments 2 weeks
  • Non-ablative light treatments (e.g. Intense Pulsed Light, light-emitting diodes) 1 month
  • Ablative skin resurfacing
  • Non-ablative dermal treatment for skin tightening (e.g. radio-frequency treatments) 6 months
  • Treatment with a BoNT-A 12 months
  • Soft tissue augmentation (e.g. biodegradable products as collagen or hyaluronic acid preparations) 24 months
  • Subjects who undergone a surgical facelift;
  • Permanent or semi-permanent dermal fillers in the forehead area;
  • Known allergy or hypersensitivity to any botulinum toxin or any component of BoNT-A (1) and/or BoNT-A (2) (see package inserts);
  • Concurrent use of treatments that affect neuromuscular transmission, such as curare-like depolarizing agents, lincosamides, polymyxins, anticholinesterases affecting the striated muscle and aminoglycoside antibiotics;
  • Pregnant women, nursing mothers, or women who are planning pregnancy during the study;

Treatment and study plan

Botulinum Toxin Type A - Azzalure

Drug

One botulinum toxin type A will be injected in one side of the forehead and the other one will be injected in the other side of the forehead at Baseline. Allocation of each BoNT-A to each side of the forehead will be randomized.

Botulinum Toxin Type A - Vistabel

Drug

One botulinum toxin type A will be injected in one side of the forehead and the other one will be injected in the other side of the forehead at Baseline. Allocation of each BoNT-A to each side of the forehead will be randomized.

Primary outcomes

  1. Severity of the Forehead Wrinkles by the Evaluator at Maximum Contraction and at Rest Using the Forehead Wrinkles Severity Scale (0 to 3) at Each Study Visit and for Each Side of the Forehead

    Time frame: 5 months : Baseline, Days 1, 2, 3, 7, 10, 14, 30, Months 4 and 5

    Bilateral comparison of forehead wrinkle severity score at rest and at maximum contraction measured by Forehead Wrinkles Severity Scale (0 to 3) at each study visit (Baseline, Days 1, 2, 3, 7, 10, 14, 30, Months 4 and 5)and for each side.

Sponsors and collaborators

Lead sponsor

Galderma R&D

Industry

Registry information

Official study title

Intra-individual Comparison of the Efficacy of Two Botulinum Toxins Type A on Moderate to Severe Forehead Wrinkles After One Injection

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Nov 17, 2009
Registry last updated
Feb 18, 2021

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.

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