Clinical trial · Interventional
Safety and Effectiveness of CATHTONG™ II PICC
A Prospective, Multicentre, Randomized, Open, Parallel Controlled Clinical Trial for Evaluating the Safety and Effectiveness of CATHTONG™ II PICC
NCT03841955CI-TRIAL-00052291completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This clinical trial is a prospective, multi-centre, open, parallel and comparative non-inferior trial design.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PICC with high pressure tolerance | Device | — | UNRESOLVED |
| rontine central venous catheter | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Experimental group
- description
- Peripheral implantation of central venous catheters and accessories with high pressure tolerance
- interventionNames
- Device: PICC with high pressure tolerance
- type
- EXPERIMENTAL
- label
- Control group
- description
- Peripheral intubation of central venous catheter
- interventionNames
- Device: rontine central venous catheter
Primary outcomes (1)
- measure
- Successful rate of one-time catheterization
- timeFrame
- Day 1
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * Subjects volunteered to participate in the trial and signed the informed consent. * Age 18 years old, 80 years old; gender is not limited; * Suitable for patients who need central venous catheterization via peripheral venipuncture (life expectancy is more than 6 months): need medium-term and long-term infusion or intravenous drug therapy; need multi-chamber infusion of multiple drugs at the same time; need infusion of irritating, corrosive or hyperosmotic drugs; hyperbaric angiography or central venous pressure monitoring function; * Patients who need to be maintained in the investigator's hospital after PICC catheterization; * Ability to communicate well with researchers and comply with test requirements. Exclusion Criteria: * Local infection of puncture vein or occlusion or serious lesion of blood vessel at puncture place; * Patients with known or suspected allergies to polyurethane; * Pre-intubation site includes trauma history, vascular surgery history, thrombosis history, radiotherapy history, bilateral breast cancer surgery affected upper limbs, superior vena cava compression syndrome, etc. * The prothrombin time was 6 seconds longer than the normal value and the activated partial thromboplastin time was 2.5 times longer than the normal value. * Pregnancy and lactation women; * The subjects had a history of difficulty in catheterization. * Patients with pacemaker implantation in vivo; * Researchers do not consider it appropriate to participate in this clinical trial.
References
Publications (0)
Data not yet available
No reference posted for this study.