Investigation of Clinical Usefulness of All-in-One Peripheral Intravenous Catheter System
- Conditions
- not Specified
- Registration Number
- JPRN-UMIN000004638
- Lead Sponsor
- ippon Becton Dickinson Company, Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 400
Not provided
Patients who have once enrolled in the Investigation. However, patients who are discharged from the study site during the study period and are again admitted are NOT excluded. Pregnant women Patients who have any one of skin inflammations, burns, other skin lesions and tattoos, etc is at or near a catheter insertion site Patients who have limited insertion sites such as the bending areas of the upper and lower extremities Patients who are in anti-cancer drug therapy Patients who are known their sensitivity to medical adhesive materials like dressing materials Patients who need antibiotics or ointment locally under the dressing material Patients who are perspirating when inserting a catheter Patients who are judged inappropriate to enroll in the Investigation by a physician or a nurse
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A re-start rate of new catheter and existing one. The re-start rate is defined that a catheter has to be removed due to any reasons including blockage of the catheter, complication such as phlebitis and the like and is replaced with a new catheter.
- Secondary Outcome Measures
Name Time Method Events including loosening or displacement of securing site or bending or kink of the catheter or phlebitis or infiltration.