3M Veraflo™ Cleanse Choice Complete™ (VFCCC) Clinical Study

Clinical Trial Summary

The purpose of this external clinical study is to demonstrate the safety and performance of the Veraflo™ Cleanse Choice Complete™ Dressing Kit which will be used in conjunction with the V.A.C.® Ulta™ Therapy Unit, utilizing V.A.C. Veraflo™ Therapy instillation functions.

See also
Status	Clinical Trial	Phase
Terminated	`NCT04163679` - Vaginal Preparation and Azithromycin to Reduce Post Cesarean Infections	N/A
Recruiting	`NCT05388591` - Evaluation of Musicotherapy on Pain During Wound Closure in the Emergency Department	N/A
Recruiting	`NCT03865147` - Single-centre Study to Investigate Safety and Efficacy of Tri-Solfen in Wound Debridement	Phase 2

See also

Status

Clinical Trial

Phase

Terminated

NCT04163679 - Vaginal Preparation and Azithromycin to Reduce Post Cesarean Infections

N/A

Recruiting

NCT05388591 - Evaluation of Musicotherapy on Pain During Wound Closure in the Emergency Department

N/A

Recruiting

NCT03865147 - Single-centre Study to Investigate Safety and Efficacy of Tri-Solfen in Wound Debridement

Phase 2

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	NCT05748392
Study type	Interventional
Source	3M
Contact
Status	Withdrawn
Phase	N/A
Start date	June 1, 2023
Completion date	June 1, 2023

3M Veraflo™ Cleanse Choice Complete™ (VFCCC) Clinical Study

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms