Peripherally Inserted Central Catheter
Conditions
Brief summary
This study is a multi-center clinical study, 3000 cases, 25 centers in the country involved, carry out the guidance of EDUG PICC standardized operation at the same period. Each center assists to use app to collect research data.The experimental data will be collected, processed and analyzed by the sponsor and the researchers, and the clinical effect of EDUG will be evaluated according to the results (like the rate of once in place, the number of adjustment times before X-ray, the length of time during the whole catheter placement, the ectopic incidence during PICC first implantation and so on, the special content can be seen in the next indicator section)
Interventions
DEVICEPICC guided by EDUG
ECG Doppler ultrasound guidance technology (EDUG) is the combination of MST puncture and ECG technology through the use of ECG Doppler ultrasound machine and valve conduction PICC to conform the localization of EDUG technology by the study of real-world
Sponsors
Qilu Hospital of Shandong University
Shandong Branden Med.Device Co.,Ltd
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patient≥18 years old 2. Follow the doctor's advice,patients who need to be placed PICC for the first time. 3. No serious cardiovascular diseases, such as atrial fibrillation,pulmonary heart disease and other P wave abnormalities, severe heart block, etc. 4. Patients who did not participate in other clinical studies； 5. Patients who volunteer to participate the clinical study, sign the informed consent and cooperate with the clinical follow-up.
Exclusion criteria
1. Patients who have partial deformity or scar formation 2. Patients whose puncture site were infected or damaged 3. Patients who have sclerosis or the cord like change of the vein 4. Patients have compressed vessel by tumor 5. Patients who are confirmed or suspected having infection, bacteremia, or sepsis related to the catheter 6. Patients whose size are not fit to insert the PICC 7. Patients who are confirmed or suspected sensitive to silica gel 8. Patients who have history of radiotherapy in the pre-insertion section 9. Patients who have history of venous thrombosis, trauma, or vascular surgery 10. Patients who have superior vena cava syndrome 11. Patients who were always not following up with the doctors 12. Patients who have severe peripheral edema 13. Patients who may be required a high flow of fluid infusion, hemodialysis, pacemaker, crutches or A-V fistulation \-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| the rate of once in place | From the date of admitting to hospital until completion of the trial, up to 6 months. | judge weather the catheter tip location guided by the EDUG is accuracy by compare the results with the Xray |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| the length of time during the whole catheter placement before X-ray | From the date of admitting until discharge to hospital, up to 14 days. | the whole length of time during the once operation guided by EDUG |
| the number of cathetering times after X-ray | From the date of admitting until discharge to hospital, up to 14 days. | the totally number of cathetering times during the operation guided by EDUG until the cather tip can be guided to the right location |
| the number of adjustment times before X-ray | From the date of admitting until discharge to hospital, up to 14 days. | the totally number of adjustment times during the once operation guided by EDUG |
| Patient acceptance | From the date of admitting until discharge to hospital, up to 14 days. | The patient who is in line with the discharge criteria and intends to enter the study shall record whether or not he has agreed to accept the operation plan and complete the operation |
| the convenience of the operation | From the date of admitting until discharge to hospital, up to 14 days. | App questionnaire was used to collect the convenience and comfort of PICC operators |
| record the adverse events | 0,24,48,72 hours and 7days after completing the whole cathetering operation; Every 7 days from completing the whole cathering operation until tube drawing whichever came first, assessed up to 1 year | the adverse events including bleeding, infection , thrombosis and so on |
Countries
China
Outcome results
None listed