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NCT04994990

Effective OnabotulinumtoxinA Dose Response Study for Upper Facial Wrinkles

Withdrawn NA Last updated 16 October 2023
What this trial tests

NA trial testing OnabotulinumtoxinA Standard Dose in Rhytides. Withdrawn.

Timeline
25 May 2023
Primary endpoint
30 November 2024
30 May 2025

Quick facts

Lead sponsorNorthwell Health
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeother
Start date25 May 2023
Primary completion30 November 2024
Estimated completion30 May 2025

Drugs / interventions tested

Conditions studied

Sponsor

Northwell Health — full company profile →

Who can join

Adults 18 to 65, any sex, with Rhytides. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This research is being done to determine if lower doses of botox than what is currently recommended can give similar results to patients, at lower cost and lower risk to them. Subjects will receive botox in the same areas of the upper face with standard doses on one side of the face. On the other side, double the botox concentration will be administered, free of charge to the participant, in order to see if the difference in concentration creates a difference in wrinkle reduction and participant satisfaction over time.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Rhytides

Currently open trials in the same condition.

Other Northwell Health trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04994990.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing