# An Investigation of Performance and Safety of the Wound Dressing FibDex in Patients With Superficial Dermal Burns

> **NCT05629091** · NA · TERMINATED · sponsor: **UPM-Kymmene Corporation** · enrollment: 7 (actual)

## Conditions studied

- Burns

## Interventions

- **DEVICE:** FibDex
- **DEVICE:** Epicite hydro
- **DEVICE:** Epiprotect

## Key facts

- **NCT ID:** NCT05629091
- **Lead sponsor:** UPM-Kymmene Corporation
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2023-08-12
- **Primary completion:** 2025-04-10
- **Final completion:** 2025-04-10
- **Target enrollment:** 7 (ACTUAL)
- **Why stopped:** UPM Kymmene Oyj announced on April 2, 2025, the closure of Biomedicals business. As a result, FibDex manufacturing and sales will discontinue. The premature termination is due to business decision, not related to any safety concerns of FibDex.
- **Last updated:** 2025-08-15

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05629091

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05629091, "An Investigation of Performance and Safety of the Wound Dressing FibDex in Patients With Superficial Dermal Burns". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT05629091. Licensed CC0.

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