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Recruiting NCT05755230

Prospective Cohort of Perioperative Results

Observational Perioperative/Postoperative Complications

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No intervention.
Who it may be relevant to
Registry conditions: Perioperative/Postoperative Complications. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Argentina
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

My Journey - Prospective Cohort of Perioperative Results

Overview

Perioperative online register of the care process and outcomes. Observational prospective cohort.

Detailed description

Center are invited to join the perioperative register where they input anonymized data about the surgical process and outcome.

Interventions

  • Other No intervention
    No intervention

Primary outcome measures

  • Perioperative International Register [Time frame: 20 years]

Eligibility criteria

Inclusion criteria

  • Patients undergoing surgery

Exclusion criteria

  • None

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Argentina · 1 center
  • COPAL — Buenos Aires

Identifiers

NCT: NCT05755230 · 1-Copal

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗