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Development of micro electric skin remover and application of Non-Surgical Skin Grafting Technology in the treatment of refractory diabetic foot ulcer

Development of micro electric skin remover and application of Non-Surgical Skin Grafting Technology in the treatment of refractory diabetic foot ulcer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031452
Enrollment
Unknown
Registered
2020-04-01
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Refractory diabetic foot ulcer

Interventions

Experimental group:Microdermabrasion + collagen hydrogel
Control group:Collagen hydrogel

Sponsors

Jiaxing Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 40-70 years old male and female; 2. The patients who were diagnosed as diabetic and had diabetic foot had been treated for 5-30 days in the early stage, and the effect of wound treatment was not good according to the judgment of clinician; 3. Patients whose total wound area is less than or equal to 1% TBSA; 4. The patients confirmed by the clinician that they need to undergo intensive dressing change and close observation before healing; 5. Patients who agree to participate in the study and sign the written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with chemical burn and electric burn induced by wound; 2. Patients with severe malnutrition and albumin < 25g / L; 3. Patients with severe systemic infection or other serious basic diseases that will affect the comparison of therapeutic effects according to the judgment of clinicians; 4. Patients with tumor, radiotherapy or chemotherapy; 5. Pregnant or lactating women and patients with family planning; 6. Patients who have participated in other clinical studies within 3 months before selection; 7. Situations that other researchers judge not suitable to participate in the study.

Design outcomes

Primary

MeasureTime frame
Wound healing rate;Wound healing time;Histopathological analysis;

Secondary

MeasureTime frame
General condition;

Countries

China

Contacts

Public ContactPan Sunfeng

Jiaxing Traditional Chinese Medicine Hospital

guozhili0316@163.com+86 15957318108

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026