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Platysma Prominence clinical trials

View clinical trials related to Platysma Prominence.

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NCT ID: NCT05773053 Completed - Platysma Prominence Clinical Trials

A Study of NT 201 Doses in the Treatment of Platysma Prominence

PAOLA
Start date: March 22, 2023
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of NT 201 in adults with moderate to severe platysma prominence.

NCT ID: NCT05134649 Completed - Platysma Prominence Clinical Trials

A Study To Assess the Safety of OnabotulinumtoxinA (BOTOX) Intramuscular Injection in Adult Participants With Platysma Prominence

Start date: November 17, 2021
Phase: Phase 3
Study type: Interventional

This is a Phase 3, open-label study to evaluate the safety of BOTOX Injection in Adult Participants with Platysma Prominence

NCT ID: NCT04994535 Completed - Platysma Prominence Clinical Trials

A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramuscular Injection in Adult Participants With Platysma Prominence

Start date: August 10, 2021
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the safety and effects of onabotulinumtoxinA (BOTOX) for the temporary improvement in the appearance of platysma prominence. Study doctors will randomize participants into 1 of the 2 groups, called treatment arms. There is a 1 in 2 chance that a participant will be assigned to placebo. Around 400 participants will be enrolled in the study across approximately 35 sites in USA, Belgium, Canada, Germany and the UK. Participants will receive a single treatment of intramuscular injection of onabotulinumtoxinA (BOTOX) or placebo on Day 1 during this 4 month long study. Participants will attend regular monthly visits during the study at the study site.

NCT ID: NCT04949399 Completed - Platysma Prominence Clinical Trials

A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramuscular Injection in Adult Participants With Moderate to Severe Platysma Prominence

Start date: July 8, 2021
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the safety and effects of onabotulinumtoxinA (BOTOX) for the temporary improvement in the appearance of platysma prominence. Study doctors will randomize participants into 1 of the 2 groups, called treatment arms. There is a 1 in 2 chance that a participant will be assigned to placebo. Around 400 participants will be enrolled in the study in the United States and Canada. Participants will receive either intramuscular injections of onabotulinumtoxinA (BOTOX) or placebo. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular monthly visits during the study at the study site.

NCT ID: NCT03915067 Completed - Platysma Prominence Clinical Trials

BOTOX® for the Treatment of Platysma Prominence

Start date: April 23, 2019
Phase: Phase 2
Study type: Interventional

To assess the efficacy and safety of BOTOX® in adults with moderate to severe platysma prominence.