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Topical continuous delivery of non-pressurised oxygen combined with negative pressure wound therapy for chronic wounds: A Randomized controlled trial

Topical continuous delivery of non-pressurised oxygen combined with negative pressure wound therapy for chronic wounds: A Randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022165
Enrollment
Unknown
Registered
2019-03-27
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-04-01

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

Conditions

chronic wounds

Interventions

control group:negative pressure wound therapy
treatment group:topical continuous delivery of non-pressurised oxygen combined with negative pressure wound therapy

Sponsors

Wound Care Center of Outpatient Department, Eastern Theater General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Chronic wounds with full cortical damage caused by various reasons (duration = 30d ), specifically including pressure injury, ulcerative wound, diabetic foot, surgical incision, traumatic wound, etc.; 2) Area = 8cm2, depth = 2cm; 3) Aged = 18 years, gender and region are not limited; 4) Patients or their families informed consent and volunteered to participate in the study.

Exclusion criteria

Exclusion criteria: 1) Malignant wounds; 2) Antibiotics are needed for systemic infections; 3) Bleeding tendency and coagulopathy; 4) Accompany with untreated osteomyelitis; 5) Accompany with nerves exposed,blood vessels exposed or active bleeding at the wound; 6) The wound is accompanied by necrotic tissue (the wound base is yellow or black) but there are debridement contraindications or inability to debride; 7) Systemic comorbidities affecting wound healing such as malnutrition, autoimmune diseases, advanced tumors, multiple organ failure, unstable blood sugar control, etc.; 8) Using steroid hormones, immunosuppressants, chemotherapeutics, etc. to affect wound healing drugs; 9) The wound can not form a closed environment; 10) Patients who have participated in other clinical trials within 3 months prior to the trial (including the interventions in this trial); 11) Sponsors or researchers or their family members who are directly involved in the trial; 12) The investigator believes that there is no reason for being selected.

Design outcomes

Primary

MeasureTime frame
Granulation tissue coverage;

Secondary

MeasureTime frame
the percentage decrease in wound surface area,wound depth;PUSH score;wound temperature;wound PH;MMP-9 expression;CD34 expression;Ki-67 expression;

Countries

China

Contacts

Public ContactJiang Qixia
jiangqixia1963@163.com+86 18900672707

Outcome results

None listed

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