Clinical Efficacy of Self-adhesive Silicone Gel Waterproof Dressings Versus Conventional Dressings in the Healing of Incisions After Total Joint Arthroplasty
Launched by FIRST AFFILIATED HOSPITAL OF XINJIANG MEDICAL UNIVERSITY · Jun 15, 2024
Trial Information
Current as of November 12, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how effective self-adhesive silicone gel waterproof dressings are compared to traditional gauze dressings for healing after total joint replacement surgery (also known as total joint arthroplasty). The goal is to find out if one type of dressing helps patients heal better and reduce the risk of infections or the need for additional surgery. To participate, individuals need to be at least 18 years old and be undergoing their first joint replacement surgery. However, those with certain health issues, such as severe infections or allergies to the silicone dressings, cannot take part.
Participants in this trial will be randomly assigned to receive either the silicone gel dressing or the conventional gauze dressing after their surgery. Researchers will monitor their healing progress over one year, checking for signs of infection and measuring how well their skin is healing. This study aims to provide valuable information that could help improve patient care and recovery after joint surgery.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age ≥18 years old, gender is not limited;
- • 2. Meet the diagnostic criteria for artificial joint replacement;
- • 3. Initial joint replacement surgery;
- • 4. Voluntary and signed informed consent.
- Exclusion Criteria:
- • 1. Allergic to self-adhesive silicone rubber waterproof dressing;
- • 2. Patients with severe knee joint infection who cannot undergo artificial joint replacement;
- • 3. Progressive renal insufficiency (stage 4 and above) or glomerular filtration rate less than 30ml/min;
- • 4. periprosthesis infection after multiple joint replacement;
- • 5. Active infection at the site of intravenous or joint injection;
- • 6. long-term use of anticoagulants or antiplatelet drugs due to other diseases;
- • 7. Have sepsis or positive blood culture within the last 30 days;
- • 8. Radiotherapy and chemotherapy are required due to neoplastic diseases;
- • 9. Receiving systemic glucocorticoid therapy (prednisone \> 10mg/ day or equivalent hormone medication);
- • 10. severe immunodeficiency diseases (such as stage 3 HIV, sickle cell anemia, splenectomy, etc.);
- • 11. Have a history of drug abuse;
- • 12. Treatment of bone marrow or other transplants with immunosuppressive drugs;
- • 13. Pregnant, parturient and lactating women;
- • 14. Participating in other clinical trials;
- • 15. Researchers believe that other reasons are not appropriate for clinical trial participants.
About First Affiliated Hospital Of Xinjiang Medical University
The First Affiliated Hospital of Xinjiang Medical University is a leading healthcare institution dedicated to advancing medical research and improving patient care through innovative clinical trials. As a prominent clinical trial sponsor, the hospital leverages its extensive expertise and state-of-the-art facilities to conduct rigorous studies across various therapeutic areas. Committed to ethical standards and patient safety, the hospital collaborates with a network of experienced researchers and healthcare professionals to foster scientific advancements and contribute to the global medical community. Its mission is to enhance healthcare outcomes while ensuring the highest quality of clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Li Cao
Study Chair
The first affliated hospital, Xinjiang medical university
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported