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Clinical Trials in Italy / NCT06725797
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Study on the Effectiveness of Hypothermal Sulphurous Water in Wound Hygiene

NCT06725797 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2024-10-20
Last updated
2024-12-10

Condition(s) studied

UlcersWound - in Medical CareWounds and InjuriesWound HealingWound CareVenous UlcersWound Cleansing

Investigational drug(s) / intervention(s)

wound hygiene with hypothermal sulfurous water by packswound hygiene with hypothermal sulfurous water by limb full immersion

wound hygiene with hypothermal sulfurous water by packs: GROUP A: After dressing removal, the wound is exposed. Sulphur thermal water at spring temperature (23°C) is applied for 20 minutes on the untreated wound by packs on non woven gauzes entirely covering the area. Eventually, if dried, gauzes are externally watered with additional sulphurous thermal water during the 20 minutes. After water application the wound follows the other 3 steps of the wound hygiene protocol: non viable tissue removal, edges reactivation and dressing. Non interactive dressings, just for wound moisture management, are used on cleaned wound/s. Dressing fixation, elastic bandages or off-load will be provided when required. the intervention will be repeated every 48 hours for both arms.

wound hygiene with hypothermal sulfurous water by limb full immersion: GROUP B: After dressing removal, the wound is exposed. Sulphur thermal water at spring temperature (23°C) is applied for 20 minutes on the untreated wound by limb full immersion in a limb tub. After the immersion, the wound follows the other 3 steps of the wound hygiene protocol: non viable tissue removal, edges reactivation and dressing. Non interactive dressings, just for wound moisture management, are used on cleaned wound/s. Dressing fixation, elastic bandages or off-load will be provided when required. the intervention will be repeated every 48 hours for both arms.

Study summary

This is an interventional double arms pilot study on the effectiveness of hydrogen sulfide (H2S) rich and microbiologically pure spa sulphurous water, in the wound hygiene of hard-to heal wounds, set in an italian spa facility. At least 24 subjects enrolled according to selection criteria will be 1:1 randomized in two intervention groups: the former (A) undergoing pack of sulphurous water on soaked gauzes for 20 minutes, the latter (B) undergoing full limb immersion for 20 minutes. Differences among the two arms will be assessed as changes in wound microbiome, wound pH, Trans epidermal water loss (TEWL), 1000x ex-vivo microscope imaging, wound fluorescence imaging for bacterial colonization and longitudinal shifts in wound sizing and peculiar features according to the Bates-Jensen Wound Assessment Tool (BWAT). Time required for re-epithelization will be recorded together with any adverse reactions or events for both arms and compared. The study aims at assessing the effectiveness of hydrogen sulfide exogenous supply on infected or colonized hard to heal wounds and which way of administration (pack Vs immersion) could have prevailing effects.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients \>18 years old * Any comorbidities (except very severe I, II immune deficiencies) * Any systemic drug therapy * Any associated dressing (except peroxides) * Acute or chronic wounds requiring wound care treatment * Genital/oral wounds * Infected wounds, including MDR pathogens * Biofilmed wounds Exclusion Criteria: * Unexplored fistula * Enteric fistula * Exposure of fascia, vessels, bones, organs * Pyoderma Gangrenosum (monotherapy) * Implanted or penetrating devices (CVC , Port-a-cath, drainages, peritoneal dialysis, external fixators....etc.) * Exposed implants(nails, plates, internal defibrillator, Pace maker) * Local antibiotic therapy (not supported by antibiogram)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Terme di Roma Acque Albiule Bagni di Tivoli Rome

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06725797 on ClinicalTrials.gov ↗ ← All trials in Italy