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ACTIVE NOT RECRUITING
NCT04162496
NA

Restylane Refyne for Correction of Horizontal Neck Rhytides

Sponsor: Siperstein Dermatology

View on ClinicalTrials.gov

Summary

Subjects with grades ranging from 1---3 on the Transverse Neck Line Scale, will be randomized to receive up to 1cc of Restylane Refyne on one side of their neck utilizing a cannula and up to 1cc of Restylane Refyne on the other side utilizing a 30--gauge needle. On Day 30, this treatment with the same left---right assignment can be repeated if optimal correction on either side has not been achieved according to the treating investigator. Subjects will return 24--48 hours after their first treatment, to fill out questionnaires, take pictures, and to be assessed by blinded evaluators regarding adverse events. Subjects will also return 30 days after their final treatment to fill out final questionnaires, take pictures, and to be assessed by blinded evaluators regarding improvement of static rhytides.

Official title: An Evaluator -Blinded, Split-Neck, Randomized Clinical Study Investigating the Efficacy and Safety of Restylane Refyne for Correction of Static Horizontal Neck Rhytides Utilizing Either a Cannula or Needle

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

24

Start Date

2020-08-11

Completion Date

2021-09-30

Last Updated

2021-06-08

Healthy Volunteers

Yes

Interventions

DEVICE

Restylane Refyne

Injection of Restylane Refyne with a cannula on one side of the neck and a 30 guage needle on the other side.

Locations (1)

Siperstein Dermatology

Boynton Beach, Florida, United States