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NCT07239375

Intraosseous Infusion in Hematologic Critical Patients

Recruiting now Last updated 20 November 2025
What this trial tests

trial testing intra-osseous (IO) infusion needle/catheter in Intraosseous Infusions in 52 participants. Currently enrolling.

Timeline
22 November 2025
Primary endpoint
22 October 2027
23 October 2027

Quick facts

Lead sponsorShanxi Bethune Hospital
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment52
Start date22 November 2025
Primary completion22 October 2027
Estimated completion23 October 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanxi Bethune Hospital

Who can join

Adults 18 to 65, any sex, with Intraosseous Infusions. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This single-center, prospective observational study will enroll 52 critically hematology patients aged 18-65 years including agranulocytosis, thrombocytopenia, severe anemia, advanced tumors, septic shock, sepsis DIC、 severe gastrointestinal bleeding, involvement of the central nervous system or intracranial hemorrhage, patients undergoing hematopoietic stem cell transplantation,etc. Vascular access will be established via intraosseous (IO) needle placement, primarily to evaluate first-attempt puncture success rate, therapeutic efficacy, and overall survival rate. Secondary endpoints include infusion speed, hemodynamic improvement, and procedural complications such as local infection and fat embolism. The study aims to definitively assess the efficacy and safety of IO infusion as a rapidly established, "non-collapsible" alternative vascular access route in the hematologic intensive care setting.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Shanxi Bethune Hospital trials

Trials by the same sponsor.

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