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Intra-Osseous Access in Difficult Vascular Access Cases

Intra-Osseous Access in Difficult Vascular Access Cases

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05708833
Acronym
IODA
Enrollment
3
Registered
2023-02-01
Start date
2023-03-02
Completion date
2024-09-10
Last updated
2025-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemodynamic Instability

Brief summary

Thousands of peripheral venous accesses are inserted every day all over the world. Some of them, such as those inserted in emergency and / or in critical patients, are absolutely vital. In the particular context of prehospital care, the rate of failure of the first attempt to insert a peripheral venous access has been evaluated at 25%. Success rates of successive attempts were about 75%. Nevertheless, the final success rate is close to 100%. Failure or delay in obtaining venous access can be life-threatening. Thus, alternatives to peripheral venous access have been proposed including intraosseous route recently made easier by the development of an automated puncture device (EZ-IO®), but still rarely used, especially on conscious patient. Currently, the place of intraosseous venous access in critical patients is not determined.

Interventions

DEVICEIntraosseous venous access

Immediate placement of humeral intra-osseous venous access (after a first failed attempt of peripheral venous access)

DEVICEPeripheral venous access

Looking for peripheral venous access, changing the site of puncture, the caliber of the catheter and/or the operator and/or assistance tools (ultrasound, infra-red guidance...) and/or using another route (oral, rectal, subcutaneous, intramuscular route and central venous access)

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Interventional study with randomisation (1:1)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adult patient, in prehospital setting, without venous access and after failure of the first attempt to place a peripheral venous access by a senior operator (doctor or nurse) AND 2. Patient with hemodynamic failure defined as: * systolic blood pressure (SBP) \< 90 mm Hg (2 measures) or * cardiac arrest or 3. Any situation requiring intubation

Exclusion criteria

* 1- Age \< 18 years 2- Venous access already available 3- Known contra-indications to intraosseous access (i.e. bilateral lesions): * Bone fracture * Skin infection * Osteoporosis * Osteomyelitis * Local burns * Recent failed intraosseous attempt * Prior surgery * Compartment syndrome * Every other local specific situations 4- Pregnancy woman 5- Patient with no national health or universal plan affiliation coverage

Design outcomes

Primary

MeasureTime frameDescription
To demonstrate that the early recourse to the intraosseous route, from the first failure, makes it possible to obtain more quickly the correction of the failure of critical patient managed in prehospital setting.• In patients with cardiac arrest: Return of spontaneous circulation (ROSC), an average of 1 hour• In patients with cardiac arrest: Time required for a return of spontaneous circulation (ROSC). Only the first ROSC will be considered.

Secondary

MeasureTime frameDescription
To determine the length of stay in hospitalDays 28Length of stay in hospital
To evaluate morbidity depending on the strategy used.In patients with cardiac arrest: Return of spontaneous circulation (ROSC), an average of 1 hourNon-functional venous
To characterize the conditions for implementation of the procedure, depending on the strategy used.1 minuteFailure to place the catheter defined by the absence of infusion or by withdrawal of the catheter within one minute after the opening of the infusion
To evaluate the patient's feedback, depending on the strategy used.Immediately after the insertion of the catheter (opening of the perfusion) and on arrival at the hospital, In patients with hemodynamic failure: Reach a systolic blood pressure correction, an average of 1 hourEvaluation of procedural pain on an analog visual scale, EVA, simple verbal scale, EVS or numerical scale, EN (from 0 to 100, the higher is the worse) In the case of patient with cardiac arrest, only the operator satisfaction will be assessed.
To evaluate the team's feedback, depending on the strategy used.Immediately after the insertion of the catheter (opening of the perfusion) and on arrival at the hospital, In patients with hemodynamic failure: Reach a systolic blood pressure correction, an average of 1 hourOperator satisfaction assessed (EVA, EVS or EN) after the placement of the catheter and on arrival at the hospital (from 0 to 100, the higher is the worse).
To evaluate mortality depending on the strategy used.Days 28Death

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026