not Specified
Conditions
Interventions
None listed
Sponsors
Nippon Becton Dickinson Company, Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who are expected to catheter insertion more than 72 hours Catheter insertion can be done at the back of the hand, forearm, upper arm or leg
Exclusion criteria
Exclusion criteria: 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| Events including loosening or displacement of securing site or bending or kink of the catheter or phlebitis or infiltration. | — |
Countries
Japan
Contacts
Public ContactTakeshi Tomaru
Nippon Becton Dickinson Company, Ltd. Clinical Development, Medical Affairs
Outcome results
None listed