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OpenTrials
Completed

NCT Number: NCT07418073

Transcutaneous CO₂ Therapy in Recurrent Hard-to-Heal Diabetic Foot Ulcers

Recurrent and hard-to-heal diabetic foot ulcers (DFUs) represent a clinically challenging subgroup with delayed closure and frequent non-response to standard of care (SOC). Impaired local perfusion and superficial tissue hypoxia, commonly attributed to microcirculatory dysfunction, are proposed contributors to impaired wound-bed progression and prolonged healing trajectories in diabetes. Transcutaneous gaseous carbon dioxide (CO₂) therapy is a non-invasive adjunct intervention with a mechanistic rationale to modulate local microcirculation and tissue oxygenation; however, controlled clinical evidence in recurrent, hard-to-heal DFUs remains limited. This prospective, randomized, controlled, open-label, parallel-group clinical investigation compares transcutaneous CO₂ therapy plus SOC versus SOC alone over 4 weeks. The primary objective is to determine whether the proportion of completely healed DFUs at Week 4 differs between groups under a predefined healing confirmation procedure. Key secondary objectives include quantifying changes in superficial tissue oxygenation (StO₂) using hyperspectral imaging and assessing pain intensity (NPRS). Supportive outcomes include ulcer area reduction metrics and wound-bed appearance in unhealed.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UMC Ljubljana

Ljubljana, Slovenia, 1000

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diabetes mellitus type 1 or 2
  • recurrent hard to heal DFU

Exclusion criteria

  • KOPD stage IV
  • CKD stage IV
  • malignant diseases
  • pregnancy
  • infected ulcer at baseline
  • inability to comply with visits

Treatment and study plan

transcutaneous application of gaseous CO2 on lower part of the body

Other

Participants in the intervention group received SOC alongside 20 sessions of CO₂ therapy. These 50-minute sessions were administered once daily on weekdays (Monday-Friday) over a 4-week period. CO₂ therapies were performed using the medical device. The participant's lower body was sealed in a single-use, biocompatible, medical-grade wrap. The wrap was filled with medical-grade CO₂ to a 99.9% concentration for a 50-minute session. After 50 minutes, CO₂ was pumped out and the wrap removed.

Primary outcomes

  1. complete ulcer healing

    Time frame: 4 weeks

    full epitelization without exudate confirmed at 2 consecutive exams

Secondary outcomes

  1. change in StO2

    Time frame: 4 weeks

    StO₂ (%) will be measured using Hyperspectral Imaging (by TIVITA HSI device) at baseline and weeks 1, 2, 3, and 4. The outcome is change from baseline in StO₂ (%). Higher values indicate better tissue oxygenation/perfusion.

  2. change in pain intensity (NPRS)

    Time frame: 4 weeks

    Change from baseline in pain intensity assessed by the Numeric Pain Rating Scale (NPRS)Outcome Measure Description: Pain intensity will be self-reported using the Numeric Pain Rating Scale (NPRS), an 11-point scale from 0 = no pain to 10 = worst imaginable pain. The outcome is change from baseline in NPRS score at week 4.

Sponsors and collaborators

Lead sponsor

University Medical Centre Ljubljana

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Feb 18, 2026
Registry last updated
Feb 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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