# A Multi-center, Randomized, Subject Blind, Active Controlled Design Clinical Study to Evaluate the Efficacy and Safety of Volus as Compared to PowerFill® for Temporary Penile Enhancement

> **NCT02833532** · PHASE3 · COMPLETED · sponsor: **Hugel** · enrollment: 68 (estimated)

## Conditions studied

- Penile Enhancement

## Interventions

- **DEVICE:** Volus/Powerfill

## Key facts

- **NCT ID:** NCT02833532
- **Lead sponsor:** Hugel
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2015-06
- **Primary completion:** 2017-01
- **Final completion:** 2017-06
- **Target enrollment:** 68 (ESTIMATED)
- **Last updated:** 2017-08-08

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02833532

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02833532, "A Multi-center, Randomized, Subject Blind, Active Controlled Design Clinical Study to Evaluate the Efficacy and Safety of Volus as Compared to PowerFill® for Temporary Penile Enhancement". Retrieved via AI Analytics 2026-06-24 from https://api.ai-analytics.org/clinical/NCT02833532. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
