Clinical Trials Logo

Glabellar Frown Lines clinical trials

View clinical trials related to Glabellar Frown Lines.

Filter by:

NCT ID: NCT02334436 Completed - Clinical trials for Glabellar Frown Lines

A Phase III Study to Demonstrate the Safety and Efficacy of DWP-450 to Treat Glabellar Lines - EV-002

EV-002
Start date: January 2015
Phase: Phase 3
Study type: Interventional

The primary objective is to demonstrate the safety and efficacy of DWP-450 (Botulinum purified neurotoxin, Type A) Injection in the treatment of moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity in adult subjects

NCT ID: NCT02334423 Completed - Clinical trials for Glabellar Frown Lines

A Phase III Study to Demonstrate the Safety and Efficacy of DWP-450 to Treat Glabellar Lines - EV001

Start date: January 2015
Phase: Phase 3
Study type: Interventional

The primary objective is to demonstrate the safety and efficacy of DWP-450 (Botulinum purified neurotoxin, Type A) Injection in the treatment of moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity in adult subjects

NCT ID: NCT02303002 Completed - Clinical trials for Glabellar Frown Lines

Efficacy and Safety of Botulinum Toxin Type A for Injection to Treat Glabellar Lines

Start date: December 2014
Phase: Phase 2
Study type: Interventional

This is a safety and efficacy study of botulinum toxin type A in subjects with glabellar frown lines.

NCT ID: NCT02236312 Completed - Clinical trials for Glabellar Frown Lines

Safety and Efficacy Study of Botulinum Toxin for the Treatment of Glabellar Frown Lines

Start date: September 2014
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to evaluate the efficacy in wrinkle reduction of a single treatment of three different doses of botulinum toxin compared to placebo, in the treatment of moderate to very severe glabellar frown lines.

NCT ID: NCT02184988 Completed - Clinical trials for Glabellar Frown Lines

Safety Study of DWP-450 (Botulinum Purified Neurotoxin, Type A) Injection to Treat Glabellar Lines

EV-004
Start date: August 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to demonstrate the safety of multiple doses of DWP-450 (Botulinum purified neurotoxin, Type A) Injection in treatment of moderate to severe glabellar lines in adult subjects.

NCT ID: NCT02108158 Completed - Clinical trials for Glabellar Frown Lines

A Safety and Efficacy Study of Different Injections Volumes of Botulinum Toxin Type A, Azzalure, in the Glabellar Lines

Start date: April 2014
Phase: Phase 4
Study type: Interventional

A randomized, evaluator-blinded, comparative, study to evaluate the efficacy and safety of different injection volumes of botulinum toxin type A, Azzalure, in the glabellar lines.

NCT ID: NCT02096081 Completed - Clinical trials for Glabellar Frown Lines

The Treatment of Glabellar Frown Lines

Start date: February 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to show that two FDA-approved botulinum toxin drugs called Xeomin® and Botox® can reduce the severity of vertical lines (wrinkles) that appear between the eyebrows (glabellar frown lines).

NCT ID: NCT01808742 Completed - Clinical trials for Glabellar Frown Lines

Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the CRYO-TOUCH III Device

Start date: November 2012
Phase: N/A
Study type: Observational

myoscience Inc. (Redwood City, CA) has developed a device for a novel, minimally invasive facial rejuvenation procedure designed to soften hyperdynamic facial lines. The myoscience Cryo-Touch III device uses well-established principles of cryobiology to cause localized reduction in muscle activity resulting in a reversible reduction in facial animation and the appearance of facial lines. The device operates on well-established cryobiology principles; that localized exposure to controlled low temperature conditions can alter tissue function. The therapy treats targeted motor nerves with low temperatures via a cold probe in the form of an assembly of small diameter needles, creating a highly localized treatment zone around the probe. The thermal algorithm is designed to produce a reversible loss of nerve conduction resulting in a temporary decrease in muscle contractility. Prior studies of Cryo-Touch, Cryo-Touch II and Cryo-Touch III have provided strong evidence of effectiveness and safety for applications in this indication. The goal of the study described herein is to investigate optimized algorithms and ongoing safety and effectiveness.

NCT ID: NCT01801826 Completed - Clinical trials for Glabellar Frown Lines

A Prospective Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the Cryo-Touch IV Device

Start date: January 2013
Phase: N/A
Study type: Observational

myoscience Inc. (Redwood City, CA) has developed a device for a novel, minimally invasive facial rejuvenation procedure designed to soften hyperdynamic facial lines. The myoscience Cryo-Touch IV device uses well-established principles of cryobiology to cause localized reduction in muscle activity resulting in a reversible reduction in facial animation and the appearance of facial lines. The device operates on well-established cryobiology principles; that localized exposure to controlled low temperature conditions can alter tissue function. The therapy treats targeted motor nerves with low temperatures via a cold probe in the form of an assembly of small diameter needles, creating a highly localized treatment zone around the probe. The thermal algorithm is designed to produce a reversible loss of nerve conduction resulting in a temporary decrease in muscle contractility. Prior studies of Cryo-Touch, Cryo-Touch II and Cryo-Touch III have provided strong evidence of effectiveness and safety for applications in this indication. The goal of the study described herein is to show the safety and effectiveness of this approach using the Cryo-Touch IV device.

NCT ID: NCT01485601 Completed - Clinical trials for Glabellar Frown Lines

Safety and Efficacy Study of Botulinum Toxin Type A to Treat Glabellar Lines

Start date: December 7, 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find an optimal dose to determine the safety and tolerability of a single dose of MT10109(clostridium botulinum type A) administered by intramuscular injection in subjects with glabellar lines compared with the standard dose of BOTOX®