# An Efficacy and Safety 6-months Study of SYNOLIS VA 80/160 and SYNOLIS VA 40/80 in the Treatment of Symptomatic Knee Osteoarthritis

> **NCT05829798** · NA · COMPLETED · sponsor: **Aptissen SA** · enrollment: 82 (actual)

## Conditions studied

- Osteoarthritis, Knee

## Interventions

- **DEVICE:** SYNOLIS VA 80/160
- **DEVICE:** SYNOLIS VA 40/80

## Key facts

- **NCT ID:** NCT05829798
- **Lead sponsor:** Aptissen SA
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2021-01-14
- **Primary completion:** 2021-10-01
- **Final completion:** 2021-10-01
- **Target enrollment:** 82 (ACTUAL)
- **Last updated:** 2023-04-26

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05829798

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05829798, "An Efficacy and Safety 6-months Study of SYNOLIS VA 80/160 and SYNOLIS VA 40/80 in the Treatment of Symptomatic Knee Osteoarthritis". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT05829798. Licensed CC0.

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