Effect of Metal Skin Sensitivity on Restenosis After Stent Implantation

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Single Group Assignment, Masking: Open Label

See also
	Status	Clinical Trial	Phase
	Terminated	`NCT00244647` - A Phase 1b Study Evaluating RESTEN-MP in Subjects With Focal de Novo Stenosis	Phase 1
	Recruiting	`NCT04862052` - Optimal Treatment for Coronary Drug Eluting Stent In-stent Restenosis	N/A

See also

Status

Clinical Trial

Phase

Terminated

NCT00244647 - A Phase 1b Study Evaluating RESTEN-MP in Subjects With Focal de Novo Stenosis

Phase 1

Recruiting

NCT04862052 - Optimal Treatment for Coronary Drug Eluting Stent In-stent Restenosis

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	NCT00226525
Study type	Interventional
Source	Hadassah Medical Organization
Contact
Status	Active, not recruiting
Phase	N/A
Start date	February 2005
Completion date	August 2006

Effect of Metal Skin Sensitivity on Restenosis After Stent Implantation

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms