- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05887089
Analytical Impact of the Transport of Pathological Biological Material by Drone (PATH-AIRCHU)
September 30, 2025 updated by: Centre Hospitalier Universitaire, Amiens
Verification of the Absence of Analytical Impact of the Transport of Pathological Biological Material by Drone Within the Amiens-Picardie University Hospital
The Hospital Group of Territory Somme Littoral Sud, through its biology sector and in partnership with the company DELIVRONE, aims to engage in the experiment of transporting biological samples by means of a drone platform.
Transport by air will be between the CHAM, the Abbeville Hospital and the CHU Amiens-Picardie by flying as much as possible over the waterways via the Somme.
With a flight speed of around 100km/h at an altitude between 80 and 120 m, drones will be able to connect sites in less than an hour by transporting packages between 2 and 3 kg.
Powered by propellers connected to rechargeable batteries, these drones do not emit CO2.
This type of transport has not been validated in France by measuring the analytical impact of transport constraints for medical biology, and has never been evaluated according to the criteria of ISO 15189 standard allowing the certification of medical biology laboratories.
Validation steps of this transportation method are therefore necessary on pathological samples prior to routine use.
The aim of the project is to verify the absence of analytical impact of the transport of pathological biological samples by drone under defined flight conditions, according to the ISO15189 norm.
Study Overview
Study Type
Observational
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Picardie
-
Amiens, Picardie, France, 80054
- CHU Amiens Picardie
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
If eligible for the study, patients from the central blood collection unit and the day hospitals of the CHU Amiens-Picardie will be offered to participate in the study.
After information and consent of the patient, blood sampling will be performed to obtain the samples necessary for the normal medical management of the patient, as well as additional tubes corresponding to the same prescribed analyses.
The collection of the extra tubes will therefore be done at the same time as the routine collection, without any additional invasive procedure.
Description
Inclusion Criteria:
- Patients admitted to the Amiens-Picardie University Hospital and having benefited from medical biology examinations including the parameters of interest
- according to the usual management modalities and without additional sampling
- at the time of the test period
Exclusion Criteria:
- Refusal to participate in the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
no intervention
|
|
|
drone transportation
|
additional transport of samples at room temperature by drone (departure from the CHU Amiens-Picardie, 1 hour flight in the CHU Amiens-Picardie air perimeter, return to the CHU Amiens-Picardie)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
variation of ASAT concentration between both groups
Time Frame: one day
|
one day
|
|
variation of ALAT concentration between both groups
Time Frame: one day
|
one day
|
|
variation of BNP concentration between both groups
Time Frame: one day
|
one day
|
|
variation of LDH concentration between both groups
Time Frame: one day
|
one day
|
|
variation of Glucose concentration between both groups
Time Frame: one day
|
one day
|
|
variation of Troponin concentration between both groups
Time Frame: one day
|
one day
|
|
variation of Potassium concentration between both groups
Time Frame: one day
|
one day
|
|
variation of HIL concentration between both groups
Time Frame: one day
|
one day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 22, 2023
Primary Completion (Estimated)
September 1, 2023
Study Completion (Estimated)
September 1, 2023
Study Registration Dates
First Submitted
May 24, 2023
First Submitted That Met QC Criteria
May 24, 2023
First Posted (Actual)
June 2, 2023
Study Record Updates
Last Update Posted (Estimated)
October 6, 2025
Last Update Submitted That Met QC Criteria
September 30, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- PI2023_843_0030
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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