AzTrials
AzTrials

SepsisMOTION-SepsisNCT07817043

Microbiology Operations & Time Optimization in Sepsis

An observational study of Sepsis and Bloodstream Infection, run by University Medicine Greifswald at 1 site in Germany.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

Trial summary

The goal of this study is to simulate turn-around times of blood cultures from blood culture collection to final communication of the result. The main objective is to develop a web-based tool that is able to simulate heterogeneous laboratory settings and to analyse the impact of infrastructure and opening hours on… Read more about this study

Who is it for?
Any age
What is being tested?
laboratory infrastructure
How many people
1,000 participants
Where
1 siteGermany
Study dates
1 Oct 2026to 1 Oct 2028
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
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: microbiological laboratories

microbiological laboratories conducting blood culture analysis

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Christian S Scheer, MD contact

christian.scheer@med.uni-greifswald.de

Evgeny A Idelevich, MD, Prof. contact

Evgeny.Idelevich@med.uni-greifswald.de

Germany1 site
  • University Medicine Greifswald

    Greifswald

Other trials in Germany

About this study

Official title: A Simulation Platform for Optimising Blood Culture Diagnostics in Sepsis

The goal of this study is to simulate turn-around times of blood cultures from blood culture collection to final communication of the result. The main objective is to develop a web-based tool that is able to simulate heterogeneous laboratory settings and to analyse the impact of infrastructure and opening hours on blood culture turn-around times.

Read the detailed description

will follow

Being tested
laboratory infrastructure
Keywords
Sepsis, blood cultures, opening hours, infrastructure, microbiology, laboratory, simulation
Medical subject headings
Sepsis, Bacterial Infections, Shock, Septic, Bacteremia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • laboratory infrastructureDiagnostic test

    will follow

What is being measured

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

  1. Turn-around time

    Measured: 4 weeks for the conduction of the simulation

Timeline

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

  1. First posted14 Sep 2026
  2. Study start1 Oct 2026 (estimated)
  3. Primary completion1 Oct 2027 (estimated)
  4. Study completion1 Oct 2028 (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
Other
Time perspective
Prospective
Enrolment
1,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07817043
Sponsor's protocol ID
Motion01
Acronym
MOTION-Sepsis
Status last verified
Sep 2026
First submitted
8 Sep 2026
Last updated
14 Sep 2026
Results posted
No
Data monitoring committee
No
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 Sepsis and Bloodstream Infection, run by University Medicine Greifswald at 1 site in Germany.

The full registered description is in the About this study section and the official record.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 14 Sep 2026. 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 Germany. 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?

Contact Christian S Scheer, MD (christian.scheer@med.uni-greifswald.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Turn-around time (time frame: 4 weeks for the conduction of the simulation). 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 14 Sep 2026; AzTrials last refreshed its copy on 27 Oct 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in