A Comparative, Retrospective Chart Review of Intended Dwell Time of a PICC

Clinical Trial Description

Subjects would have received a 4 Fr Single Lumen PICC line between Aug 2020 and Oct 2020. The two groups will be HydroPICCs and the standard of care for the facility. A comparison of multiple endpoints will be evaluated between the two groups. ;

Study Design

Related Conditions & MeSH terms

See also
	Status	Clinical Trial	Phase
	Enrolling by invitation	`NCT05702515` - Vascular Positioning System G4 Algorithm ECG Data Collection for Model Training Study
	Terminated	`NCT04920929` - PICC Asymptomatic Thrombosis Study: A Pilot Study	N/A

See also

Status

Clinical Trial

Phase

Enrolling by invitation

NCT05702515 - Vascular Positioning System G4 Algorithm ECG Data Collection for Model Training Study

Terminated

NCT04920929 - PICC Asymptomatic Thrombosis Study: A Pilot Study

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	NCT04656548
Study type	Observational
Source	Access Vascular Inc
Contact
Status	Completed
Phase
Start date	November 13, 2020
Completion date	April 23, 2021

A Comparative, Retrospective Chart Review of Intended Dwell Time of a PICC Line

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms