Clinical Outcome of Defect Reconstruction Using IDRT Single Layer :

See also
Status	Clinical Trial	Phase
Completed	`NCT01848821` - The Effect of OASIS Ultra on Critical Sized Wound Healing	Phase 1
Completed	`NCT04754048` - Confirm the Safety and Performance of Avance Solo NPWT System	N/A
Completed	`NCT04593693` - A Dual-center Study Evaluating Clinical Acceptance of a NPWT Wound Care System	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT01848821 - The Effect of OASIS Ultra on Critical Sized Wound Healing

Phase 1

Completed

NCT04754048 - Confirm the Safety and Performance of Avance Solo NPWT System

N/A

Completed

NCT04593693 - A Dual-center Study Evaluating Clinical Acceptance of a NPWT Wound Care System

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	NCT01704950
Study type	Observational
Source	Integra LifeSciences Services
Contact
Status	Completed
Phase	N/A
Start date	February 2013
Completion date	August 2015

Clinical Outcome of Defect Reconstruction Using IDRT Single Layer : Results From a Prospective Multicentric Trial

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms