About this trial
The goal of this observational study is to learn about the safety and effectiveness of midline catheters in patients who receive midline catheter placement as part of their routine clinical care. The main question it aims to answer is:
Do midline catheters demonstrate acceptable safety and effectiveness when used in routine clinical practice?
Participants who receive a midline catheter as part of their regular medical care will have their clinical data collected from electronic medical records and patient questionnaires, and followed for outcomes related to catheter-related complications and functional performance.
Eligibility criteria
Qualifiers
Age ≥ 18 years
First-time midline catheter placement per physician order
Not enrolled in another clinical study
Willing and able to provide informed consent and comply with follow-up (unless consent waived by local ethics committee)
Disqualifiers
Deemed unsuitable by investigator (e.g., poor compliance or inability to communicate clearly)
Refusal of informed consent by patient or family member
Trial design
Treatments tested in this trial
- Midline catheter placement
Treatment groups
Sponsors and collaborators
Shandong Branden Med.Device Co.,Ltd
Lead sponsor
Zibo Central Hospital
Collaborator