The Efficacy & Safety of SeQuent® Please in the Treatment of Small Vessel

Clinical Trial Summary

The purpose is to evaluate the safety and effectiveness of paclitaxel-releasing coronary balloon (Catheter SeQuent® Please) versus rapid exchange PTCA balloon catheter (SeQuent® Neo) in the treatment of stenoses of coronary small vessels. 270 subjects will be enrolled for the trials.

See also
	Status	Clinical Trial	Phase
	Recruiting	`NCT05300997` - Translational Immunodiagnostics in Stroke (TrImS)
	Recruiting	`NCT06159140` - Small Vessel Diseases: Ultra-realistic Microstructure Computational Model to Refine Individual Treatment	N/A

See also

Status

Clinical Trial

Phase

Recruiting

NCT05300997 - Translational Immunodiagnostics in Stroke (TrImS)

Recruiting

NCT06159140 - Small Vessel Diseases: Ultra-realistic Microstructure Computational Model to Refine Individual Treatment

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03625830
Study type	Interventional
Source	B. Braun Medical International Trading Company Ltd.
Contact	Jun Bo Ge
Phone	+86 21 64041990
Email	lcsyjg@zs-hospital.sh.cn
Status	Recruiting
Phase	N/A
Start date	December 18, 2017
Completion date	December 30, 2019

The Efficacy and Safety of SeQuent® Please in the Treatment of Small Vessel Disease (SVD) Patient

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms