Health Condition 1: L768- Other intraoperative and postprocedural complications of skin and subcutaneous tissue
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Consent provided by the patient or legal representative for participation in the study Patients who are able to tolerate non-invasive monitoring
Exclusion criteria
Exclusion criteria: Patients with previous surgical complications Patients with contraindications to the use of non-invasive sensors Patients with severe comorbidities such as cardiovascular, pulmonary, or systemic infections that could interfere with study outcomes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To develop a novel, non-invasive instrument that measures oxygen saturation, temperature, and local pressure for early detection of surgical site infections and complications in abdominal trauma patients.Timepoint: 1 year | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the effectiveness and reliability of the instrument in comparison to standard clinical methods for detecting surgical site infections, ensuring real-time monitoring and timely intervention.Timepoint: 1 year;Assess the feasibility of integrating the instrument into routine postoperative care, improving patient outcomes by enabling continuous monitoring and reducing the need for invasive diagnostic procedures.Timepoint: 1 year | — |
Countries
India
Contacts
Saveetha medical college and Hospital