Trials / Completed
CompletedNCT01849601
Effectiveness and Safety Study of Peripheral Balloon Dilatation Catheter in Percutaneous Transluminal Angioplasty(PTA) Procedure
A Prospective, Multicenter and Single-arm Target Value Clinical Study on the Efficacy and Safety of Peripheral Balloon Dilatation Catheter in PTA Procedure
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 167 (actual)
- Sponsor
- Acotec Scientific Co., Ltd · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether the peripheral balloon dilatation catheter (trade name: Iris) is safe an effective in PTA procedure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | percutaneous transluminal angioplasty balloon catheter |
Timeline
- Start date
- 2012-12-01
- Primary completion
- 2013-03-01
- Completion
- 2013-03-01
- First posted
- 2013-05-08
- Last updated
- 2015-03-23
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT01849601. Inclusion in this directory is not an endorsement.