Prospective Cohort of Perioperative Results

• Sponsor: COPAL - My Journey (Other)
• Overall Status: Recruiting
• CT.gov ID: NCT05755230
• Collaborator: (none)
• Enrollment: 50,000
• Location: 1
• Anticipated Duration (Months): 324
• Patients Per Site Per Month: 154.3

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Perioperative/Postoperative Complications	Other: No intervention

Detailed Description

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

Study Design

• Study Type: Observational [Patient Registry]
• Anticipated Enrollment: 50000 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: My Journey - Prospective Cohort of Perioperative Results
• Actual Study Start Date: Jan 1, 2023
• Anticipated Primary Completion Date: Jan 1, 2043
• Anticipated Study Completion Date: Jan 1, 2050

Outcome Measures

Primary Outcome Measures

1. Perioperative International Register [20 years]

   Collaborative register of preoperative variables

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• Patients undergoing surgery

Exclusion Criteria:

• None

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	COPAL	Buenos Aires		Argentina

Sponsors and Collaborators

• COPAL - My Journey

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Santiago Mc Loughlin, MD, COPAL - My Journey
• ClinicalTrials.gov Identifier: NCT05755230
• Other Study ID Numbers: 1-Copal
• First Posted: Mar 6, 2023
• Last Update Posted: Mar 6, 2023
• Last Verified: Feb 1, 2023

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Santiago Mc Loughlin, MD, COPAL - My Journey: Periopererative; Enhanced Recovery
• Additional relevant MeSH terms: Postoperative Complications

Study Results

No Results Posted as of Mar 6, 2023