Wound Heal Clinical Trial
Official title:
Effectiveness of Extracorporeal Shockwave Therapy in Patients With Chronic Wounds Hospitalized in a Medium Stay Hospital
NCT number | NCT06210399 |
Other study ID # | 10 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | November 1, 2023 |
Est. completion date | December 31, 2024 |
Introduction: Chronic wounds are a major health problem with impact in the quality of life of patients, increased their morbidity and mortality, nursing burden, extend the hospital stays, and healthcare costs. Searching how to apply the best care available in wounds, shock wave treatment is found in order to stimulate tissue growth in this type of skin injuries. There are different studies to support this recommendation but also there is variability about of patients, different types of injuries or settings. It is considered that more research studies are needed to maintain this evidence and to explore other settings like the effectiveness in a medium stay hospital. Objectives: To assess the effectiveness of shockwave treatment to reduce the size of chronic wounds. Method: A quasi-experimental design will be used. The population under study will include patients admitted in the Functional Recovery Unit who present chronic wounds upon admission. The sample size will be 30 patients. An intentional non-probabilistic sampling will be carried out. Main outcome: decrease the wound size. Sociodemographic variables, personal history, comorbidities, current clinical situation, shock wave treatment variables and its evolution will be collected. Applicability: In case of findings are better than habitually care, the number of treatments required by the patient would be reduced, the patient's state of health would improve, the risk of infection of the wound decrease, and the comfort and quality of life of patients could improve. The findings may represent a change in clinical practice because they may be used to modify the treatment protocols for chronic wounds at the Guadarrama Hospital and in other similar hospitals. Also, they can contribute to the evidence based care which supports shockwave treatment.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | December 31, 2024 |
Est. primary completion date | October 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patient aged 18 years or older, - To have a chronic wound classified as: - pressure ulcer, - ischemic wounds, - neuropathic wounds, - dehiscence of surgical wounds - delayed current of wound healing of more than 6 weeks. - To sign informed consent. Exclusion criteria: - To have signs of infection observed in wound. - Necrotic tissue. - Tumor wounds. - Venous thrombosis. - Large blood vessels at lesion edges. |
Country | Name | City | State |
---|---|---|---|
Spain | Laura Martín Losada | Guadarrama | Madrid |
Lead Sponsor | Collaborator |
---|---|
Guadarrama Hospital | Puerta de Hierro University Hospital |
Spain,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decrease wound size area | Decrease de size area at the end of the intervention. The surface of the wound will be measured in centimeters (length x width) | All wounds will be measured at the end of the intervention (3 weeks). | |
Secondary | To quantify the change in the size of chronic wounds treated with shock waves | The surface of the wound will be measured in centimeters. The average of the decrease will be evaluated. | at the end of the intervention (3 weeks) | |
Secondary | To identify the patients variables related to achieve a lesion reduction equal to or greater than 50% of the surface measured in centimeters (greater success in healing). | The demographic (aged, sex) and clinic (urinary incontinence, faecal incontinence, personal history, Barthel Index, Norton Scale, blood albumin, smoking habits, type of wound, location of wound, clinical course) variables will be compared with the main variable | at the end of the intervention (3 weeks) | |
Secondary | To assess number and types of side effects what patients shows related to the use of low-frequency shockwaves in chronic wounds. | Side effects (none, bleeding, skin redness, red spots, vasovagal syncope, paresthesia, hypesthesia, others) will be collected after the sessions. | at the end of the intervention (3 weeks) | |
Secondary | To assess whether the pain perception due to chronic wounds in patients undergoing the intervention decreases. The pain perception will be measured with Visual Analogue Scale (VAS) or Pain Assesment in Advanced Dementia Scale (PAINAD). | Pain will be assessed baseline and during the shockwave session with Visual Analogue Scale (VAS) or Pain Assesment in Advanced Dementia Scale (PAINAD). The tool will be used depending on the patients' cognitive status. VAS and PAINAD scales measure fron 0 to 10 being 0 without pain and 10 the worst pain possible. | Baseline and during the intervention (up 3 weeks) |
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