Clinical experience of patient-controlled analgesia using new device with micropump
- Conditions
- Patients who are eligible to start PCA after surgeries
- Registration Number
- JPRN-jRCTs062190015
- Lead Sponsor
- Shimizu Kazuyoshi
- Brief Summary
This PCA device with new micropump was clinically used for postoperative pain without any serious complications in 5 patients. Physicians who used this device satisfied with the quality of device.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 5
Patients who meet all of the following;
1)Patients who are eligible for PCA using this device intravenously or epidurally after operations under general anesthesia.
2)Age >= 20 and <80
3)Patients who undergo surgeries or procedures without public insurance
4)Patients who are able to obtain own consent by themselves
5) Patients who will admit to the Intensive Care Unit
Patients who meet at least one of the following;
1)Severe heart failure (NYHA class 3 or 4)
2)Severe respiratory failure (Hugh-Jones class 3 or 4)
3)Past history of psychiatric disease
4)Past allergic history of local anesthetics and narcotics
5)Withdraw consent before starting PCA
6)Pregnant and lactating women
7) Investigator judged to be inappropriate for this research
In case of epidural PCA
8)Severe infection on the insertion site
9)Severe coagulopathy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method