# Feasibility Study: Histological Characterization After Treatment With the Ulthera® System

> **NCT01713569** · NA · TERMINATED · sponsor: **Ulthera, Inc** · enrollment: 2 (actual)

## Conditions studied

- Skin Laxity

## Interventions

- **DEVICE:** Ulthera Treatment

## Key facts

- **NCT ID:** NCT01713569
- **Lead sponsor:** Ulthera, Inc
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2012-10
- **Primary completion:** 2013-09
- **Final completion:** 2013-10
- **Target enrollment:** 2 (ACTUAL)
- **Why stopped:** Slow subject enrollment; study to be obtained is no longer required.
- **Last updated:** 2017-11-24


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01713569

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01713569, "Feasibility Study: Histological Characterization After Treatment With the Ulthera® System". Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/clinical/NCT01713569. Licensed CC0.

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