Date of summary:

Title of clinical investigation:

Name and contact details of the entity sponsoring the study:

Name of the entity funding the study2:

Single identification number:

Prior to full functioning of EUDAMED, this will be the CIV-ID, which is obtained from the authorising competent authority.

Once EUDAMED is functional, this refers to the single identification number as referred to in Article 70(1) of MDR

Clinical investigation plan number:

Title of the clinical investigation - summary information4

Brief Study Title

Full study title3

A brief description of the design, the experimental medical device, comparator (when relevant), care provider (when relevant), and population of the clinical investigation.

Dates of investigation3

Start (the first act of recruitment in the clinical investigation) and end (the last visit of the last subject in the clinical investigation) dates of the clinical investigation5. Please see MDCG document 2021-6 for further description of these terms.

Location(s)

Where the investigation was conducted, including site location and country.

If relevant, reason for temporary halt or early termination3

Where relevant. Reasons may include positive active findings, positive control findings, safety findings, futility, slow recruitment, external evidence, etc.2

Purpose of the clinical investigation4

Brief explanation of the rationale for the clinical investigation, including:

Depending on the context of the clinical investigation, please describe:

Description of the investigational device, clinical investigation, and methods used4

Do not include any results, analysis, conclusions or discussion points in this section.

Description of participants4

Description of the eligibility criteria for participants and the settings.

Where applicable, a description of the eligibility criteria for centres involved in the investigation and those performing the interventions.

Description of the device and comparator6

Should include a description of the investigational device, its version/variant and intended purpose including the different components required for the medical intervention(s) involving the device under investigation (e.g. the pre and post-operative care, medical/surgical intervention, etc.).

For comparative studies, descriptions of both the experimental intervention and comparator should be provided.

Description of procedures to use the device9

Brief description of the procedures and methods necessary for use of the device in the clinical investigation.

Study Design4

Description and justification of the chosen study design, i.e. randomised controlled trial (parallel, cluster, crossover, factorial, non-inferiority), non-randomised comparative study, non-comparative study, other.

Objectives and endpoints 4

Brief description clearly stating the primary and secondary objectives of the investigation as well as hypotheses that were tested.

Primary and secondary endpoints should also be clearly defined.

Sample size 7

Please include the power and sample size estimations. Include adjustments made in this calculation for dropout rate/lost to follow up, where relevant.10

Randomisation and blinding8

Where relevant, a description of the methods of intervention allocation and blinding methods used (if any).

Follow up duration4

Length of time participants were followed in the study. Also indicate the intended lifetime of the device under investigation.

Concomitant treatments4

Description of any treatments that were necessary for all subjects receiving the medical device in this clinical investigation. Please explain how this may differ from usual standard of care for this medical device, if relevant.

Statistical analysis methods4

Brief description of the statistical methods used to provide outcomes’ estimates, compare groups for the primary outcome, to perform additional analyses, to adjust for biases, to deal with missing data.

Substantial modifications11

Where relevant, a table describing any substantial modifications to the clinical investigation plan, relevant versions of the clinical investigation plan and dates of these modifications. Please confirm approval from an ethics committee has been received for these modifications.

Results of the investigation4

Participant flow12

Number of participants screened, enrolled, allocated and followed up to each intervention.

The use of this or similar flowchart is strongly recommended13.

Please note, the below flowchart is for randomised two arm studies. The flowchart will need to be adjusted for different study designs.

Baseline demographic and clinical characteristics4

If available, description of age, sex, ethnic background, country, stage of disease, relevant co-morbidities and any other disease-influencing factors in participants.

When applicable, description of care providers (case volume, qualification, expertise, etc.) and centres (volume) in each group.

Outcome of the intervention4

Results on primary endpoint including in absolute numbers when feasible (e.g. 10/20, not 50 %), estimated effect size and the precision of the result. Please include whether an analysis is intention-to-treat or per protocol.

Results of secondary endpoints or additional analyses can be reported, but the dangers of drawing conclusions from these results should be discussed.

Safety outcomes 14

Description of adverse events15, adverse device effects16 and device deficiencies15Listed table in order of most to least frequent, in numerical absolute numbers (X out of YX subjects) and percentage (X% of subjects) and the nature of these events/effects (expected/unexpected).

Only aggregated information related to these events/effects should be presented.5List of any subject deaths.

Number of subjects withdrawn from the investigation and reasons.

Deviations to clinical investigation plan5

Where relevant, a description of any deviations to the clinical investigation plan which occurred during the clinical investigation

Conclusion of the clinical investigation4

What the results mean17

Brief description of the results of this investigation: overall assessment of benefits vs risks of the intervention in light of the investigation

What does this clinical investigation add to the clinical data related to the safety and performance of the device?

What do the results add to the current scientific knowledge17

Brief description of the results of this investigation in the context of current evidence: overall benefits vs risks assessment of the investigational medical device in the context of all other evidence available, and the implications of the results in clinical practice.

Limitations18

Any limitations of the investigation, such as biases in the investigation, uncertainties which remain following the investigation or limitations in the applicability of the results to real world settings

Potential for future studies18

CIV-ID

Clinical Investigation Identification (number)

EUDAMED

European Database for Medical Devices

MDR

Medical Device Regulation