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General PracticeRCIMGNCT05544617

Recurrent Collection By Medical Student in General Medicine

An observational study of General Practice, run by Sorbonne University at 1 site in France.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The project for the recurrent collection of data from interns in general medicine is a formalized description of the consultations attended by medical students during their outpatient training. This formalization uses the International Classification of Primary Care. Read more about this study

Who is it for?
Any age
Conditions the study is for
General Practice
How many people
1,000 participants
Where
1 siteFrance
Study dates
8 Jul 2022to 1 May 2024
How long will I take part?
24 Months
Phase
Observational
Are there results?
None posted in the registry

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
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: iterations of group of 5 consecutive patients consulting a general practice, regardless of the reason for consultation

Who may be able to join

  • consultation of his general practitioner

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

France1 site, 1 recruiting
  • guillaume AVENIN

    Avon, 77210

    guillaume AVENIN, 0659004035, guillaume.avenin@gmail.com

    Recruiting

Other trials in France

About this study

Official title: Recurrent Collection By Medical Student From Sorbonne-Université in General Medicine

The project for the recurrent collection of data from interns in general medicine is a formalized description of the consultations attended by medical students during their outpatient training. This formalization uses the International Classification of Primary Care. This project aims to create a research network between general medical interns, mainly for their thesis, which pools their observations in a database accessible to all participants.

Keywords
citizen science, Medical student, ICPC

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. reason for consultation

    ICPC

    Measured: through study completion, an average of 6 month

  2. diagnosis

    ICPC

    Measured: through study completion, an average of 6 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2022
  2. Study start8 Jul 2022
  3. Primary completion30 Oct 2023 (estimated)
  4. Study completion1 May 2024 (estimated)

Resources

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
Family based
Time perspective
Prospective
Enrolment
1,000 participants (estimated)
Target duration
24 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT05544617
Sponsor's protocol ID
1
Acronym
RCIMG
Status last verified
Sep 2022
First submitted
8 Sep 2022
Last updated
16 Sep 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of General Practice, run by Sorbonne University at 1 site in France.

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: status not confirmed, as of the sponsor's last update on 16 Sep 2022. 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 France. 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?

Results are not available in the source record.

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?

reason for consultation (time frame: through study completion, an average of 6 month). The study lists 2 primary outcomes in all. 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 16 Sep 2022.

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