# A Clinical Study Evaluaing the Efficacy, Safety, and Patient Satisfaction of Injectable Hylaronic Acid With 0.3% Lidocain Hydrochloride, Prevelle Silk, for Superficial, Vertical Perioral Lines and Superficial, Horizontal, Lateral Canthal Lines

> **NCT01267149** · — · UNKNOWN · sponsor: **Goldman, Butterwick, Fitzpatrick and Groff** · enrollment: 13 (estimated)

## Conditions studied

- Wrinkles

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT01267149
- **Lead sponsor:** Goldman, Butterwick, Fitzpatrick and Groff
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2010-08
- **Primary completion:** —
- **Final completion:** —
- **Target enrollment:** 13 (ESTIMATED)
- **Last updated:** 2010-12-28

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01267149

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01267149, "A Clinical Study Evaluaing the Efficacy, Safety, and Patient Satisfaction of Injectable Hylaronic Acid With 0.3% Lidocain Hydrochloride, Prevelle Silk, for Superficial, Vertical Perioral Lines and Superficial, Horizontal, Lateral Canthal Lines". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT01267149. Licensed CC0.

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