Perioperative/Postoperative ComplicationsNCT05755230
Prospective Cohort of Perioperative Results
An observational study of Perioperative/Postoperative Complications, run by COPAL - My Journey at 1 site in Argentina.
Trial summary
Perioperative online register of the care process and outcomes. Observational prospective cohort. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Perioperative/Postoperative Complications
- How many people
- 50,000 participants
- Where
- 1 siteArgentina
- Study dates
- 1 Jan 2023to 1 Jan 2050
- How long will I take part?
- 20 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Patients undergoing surgery.
Who may be able to join
- Patients undergoing surgery
Who cannot join
- None
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Argentina1 site, 1 recruiting
- Recruiting
COPAL
Buenos Aires
Adrian O Alvarez, MD, 54 9 11 5137 0347, tatotatun@gmail.com
About this study
Official title: My Journey - Prospective Cohort of Perioperative Results
Perioperative online register of the care process and outcomes. Observational prospective cohort.
Read the detailed description
Center are invited to join the perioperative register where they input anonymized data about the surgical process and outcome.
- Being tested
- No intervention
- Keywords
- Periopererative, Enhanced Recovery
- Medical subject headings
- Postoperative Complications
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
No interventionOther
No intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
Perioperative International Register
Collaborative register of preoperative variables
Measured: 20 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Mar 2023
- Study start1 Jan 2023
- Primary completion1 Jan 2043 (estimated)
- Study completion1 Jan 2050 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Perioperative/Postoperative ComplicationsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 50,000 participants (estimated)
- Target duration
- 20 Years
Sponsor and investigators
- Lead sponsor
- COPAL - My Journey
- Sponsor type
- Research network
- Responsible party
- Principal investigator, Santiago Mc Loughlin, COPAL - My Journey
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05755230
- Sponsor's protocol ID
- 1-Copal
- Status last verified
- Feb 2023
- First submitted
- 23 Feb 2023
- Last updated
- 6 Mar 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 6 Mar 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- My Journey - Prospective Cohort of Perioperative Results
- ClinicalTrials.gov ID
- NCT05755230
- Acronym / sponsor ID
- 1-Copal
- Keywords
- Periopererative, Enhanced Recovery
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 50,000 participants (estimated)
- Lead sponsor
- COPAL - My JourneyResearch network
- Study start
- 1 Jan 2023 (actual)
- Primary completion
- 1 Jan 2043 (estimated)
- Study completion
- 1 Jan 2050 (estimated)
- First posted
- 6 Mar 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 20 Years
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients undergoing surgery.
Key inclusion criteria (1 listed)
- Patients undergoing surgery
Key exclusion criteria (1 listed)
- None
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| No interventionNo intervention | Other | – |
Primary outcome
Perioperative International Register
Time frame: 20 years
Collaborative register of preoperative variables
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Mar 2023.
- Individual participant dataSharing planned: Undecided
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Perioperative Dutasteride for Hemorrhage Control in Bipolar TURP Under Anticoagulation.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Perioperative/Postoperative Complications, run by COPAL - My Journey at 1 site in Argentina.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 6 Mar 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Argentina. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Perioperative International Register (time frame: 20 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Mar 2023.