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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03329768
Other study ID # 2016-15
Secondary ID 2016-A00673-48
Status Completed
Phase
First received
Last updated
Start date September 28, 2016
Est. completion date June 2, 2023

Study information

Verified date June 2023
Source Assistance Publique Hopitaux De Marseille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A preliminary study was conducted from 01/26/2015 to 10/26/2015 on 605 patients admitted to MIA with an intravenous and/or a urinary catheter. the investigators analyzed: - the demographic characteristics of the patient - the final diagnosis - the patient's severity and the patient outcome after discharge from MIA - the justification of the venous and or a urinary catheter - the duration of the prescription of the device Evaluation on admission of the need to maintain an intravenous or urinary catheter. Adjusting the prescription in terms of duration or withdrawal of the device in order to limit their complications (lymphangitis, superficial thrombophlebitis, bacteremia related to health care, urinary tract infection). Hypothesis: Limit the length of stay and reduce the cost of hospitalization.


Recruitment information / eligibility

Status Completed
Enrollment 3000
Est. completion date June 2, 2023
Est. primary completion date January 25, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient with an intravenous catheter and/or a urinary catheter. - Patient is more than 18 years old. - Patient who accepts to have his medical records reviewed for research. - Patient with health insurance Exclusion Criteria: - Refusal of participation in the study

Study Design


Locations

Country Name City State
France Assistance Publique Hopitaux de Marseille Marseille

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of patients with intravenous catheter 3 YEARS
Primary number of patients with urinary catheter 3 YEARS