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Smart app for Monitoring the Orthopaedic Postoperative Complications

Evaluation of Effectiveness using Mobile based Application Versus Conventional follow up of Orthopaedic Post-operative Patients and Prevent their Post-operative Complications - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/03/083566
Enrollment
100
Registered
2025-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: mobile application POC: Patients undergoing orthopedic surgeries will use the mobile application POC as part of their post-operative care protocol. The app offers personalized guidance

Sponsors

visnu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged eighteen years and above. Patients who underwent elective orthopedic surgeries following trauma. Patients who have access to a mobile device (smartphone or tablet) and are able to use it to interact with the mobile application. Patients who provided informed consent for participation in the study.

Exclusion criteria

Exclusion criteria: Patients with active infections as surgery or intervention can exacerbate the infection. Patients with suppressed immune systems due to diseases like HIV/AIDS, or immunosuppressive therapies, who have high risk of developing infections after surgery. Patients with open trauma, vascular or nerve compromise, significant bone loss Patients with cognitive impairments that could interfere with app usage or follow-up compliance. Patients with comorbid conditions that may affect post-operative recovery (e.g., severe cardiovascular diseases). Patients who were non-ambulatory before surgery. Patients lacking access to a compatible mobile device (e.g., smartphone or tablet) or reliable internet service. Patients undergoing surgeries or treatments for non-orthopedic conditions that may affect recovery and postoperative outcomes related to orthopedic surgery. Patients with severe, uncontrolled medical conditions (e.g., advanced heart disease, chronic respiratory conditions) that might significantly impact their postoperative recovery or complicate the follow-up process. Patients with psychiatric conditions. Patients currently participating in other clinical trials that might interfere with or confound the results of this study, particularly those involving postoperative care or recovery.

Design outcomes

Primary

MeasureTime frame
Effectiveness in Preventing Post-Operative Complications: The primary outcome is to evaluate the effectiveness of the mobile-based application in preventing orthopedic post-operative complications, such as infections, deep vein thrombosis, and non-union, compared to conventional follow-up methods. Rate of Complication Detection: The primary outcome is to assess the rate at which post-operative complications are detected through the mobile application versus conventional follow-up methods during the post-operative period.Timepoint: at 4 weeks post op

Secondary

MeasureTime frame
Time to Detection of Complications: The secondary outcome is to compare the time taken to identify post-operative complications using the mobile-based application versus conventional follow-up methods. Patient Satisfaction with Monitoring Methods: The secondary outcome is to assess patient satisfaction with the mobile-based application compared to conventional follow-up methods, measured through a standardized satisfaction survey or questionnaire. Follow-up Adherence: The secondary outcome is to measure adherence to follow-up schedules, comparing the percentage of patients who engage with the mobile application versus those who attend conventional follow-up appointmentsTimepoint: at 12 weeks post op

Countries

India

Contacts

Public ContactNitesh kumar rathi

Saveetha medical college and hospital

niteshrathi73@gmail.com9840136713

Outcome results

None listed

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