# A Non-randomized, Open-Label Study to Evaluate the Safety and Effectiveness of Insight® Pro Device for Evaluating Lymphatic and Venous Disorders (VOLGA)

> **NCT05628688** · — · COMPLETED · sponsor: **Koya Medical, Inc.** · enrollment: 67 (actual)

## Conditions studied

- Lymphedema
- Chronic Venous Insufficiency
- Edema
- Venous Insufficiency of Leg

## Interventions

- **DIAGNOSTIC_TEST:** Insight Pro Device for Diagnosis

## Key facts

- **NCT ID:** NCT05628688
- **Lead sponsor:** Koya Medical, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2023-08-08
- **Primary completion:** 2024-08-28
- **Final completion:** 2025-12-04
- **Target enrollment:** 67 (ACTUAL)
- **Last updated:** 2025-12-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05628688

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05628688, "A Non-randomized, Open-Label Study to Evaluate the Safety and Effectiveness of Insight® Pro Device for Evaluating Lymphatic and Venous Disorders (VOLGA)". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT05628688. Licensed CC0.

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