Postoperative Follow-up Via Artificial Intelligence-Based Application Versus Automated Messaging Application in Patients Receiving Continuous Regional Analgesia: A Comparative Study
Sponsor: Pontificia Universidad Catolica de Chile
Trial Details
| Condition | Anesthesia, Anesthesia , Analgesia, Regional Anesthesia, Regional Anesthesia Success |
| Intervention | AI-driven follow-up platform; Satisfaction; Adherence to the follow-up protocol; Response rates from postoperative days one through three |
| Phase | NA |
| Status | Not_yet_recruiting |
| Participants | 166 |
| Est. Completion | 1 July 2026 |
| Last Updated | 3 Apr 2026 |
Primary Outcome
Comparison of patient-initiated inquiry rates between AI-App and Control-App
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Patients aged between 18 and 75 years. * Physical status classification ASA I or II. * Scheduled for ambulatory surgical programs at UC Christus Health Network centers (Hospital Clínico, Clínica San Carlos de Apoquindo, or Centro Médico Santa Lucía). * Patients receiving postoperative pain management via continuous peripheral nerve block (CPNB) with a perineural catheter and disposable infusion pump. * Ownership and documented proficiency in operating a smartphone to access the mobile application. * Provision of written informed consent. Exclusion Criteria: * Inability to understand or follow the digital monitoring protocol. * Patients not meeting the age or ASA physical status requirements.
Trial Sites
Countries
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