RECRUITING

Central Line Study

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Two different techniques for placing a central venous catheter will be compared. The studyu team hypothesizes that clinicians randomized to the peripheral catheter technique will have higher first attempt success rates, fewer procedural complications, and a shorter mean time to procedure completion than physicians assigned to wire through hollow bore needle.

Official Title

A Randomized Study Comparing Two Techniques for Central Venous Catheter Insertion

Quick Facts

Study Start:2022-11-16
Study Completion:2027-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05534971

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. * Inherited, acquired, or medication related coagulopathy or thrombocytopenia (platelets \< 100,000). Patients will not be excluded for use of aspirin or other anti-platelet medication.
  2. * Previous central venous access at the same anatomical site.
  3. * Any indwelling catheter or wire that could potentially interfere with central line placement
  4. * Anterior border of the target vein deeper than 3.5cm

Contacts and Locations

Study Contact

Joe Offenbacher, MD
CONTACT
646-929-7815
joseph.offenbacher@nyulangone.org
Benjamin Friedman, MD
CONTACT
718-920-6626
bfriedm@montefiore.org

Principal Investigator

Benjamin J Friedman, MD
PRINCIPAL_INVESTIGATOR
Montefiore Medical Center

Study Locations (Sites)

Montefiore
Bronx, New York, 10467
United States

Collaborators and Investigators

Sponsor: Montefiore Medical Center

  • Benjamin J Friedman, MD, PRINCIPAL_INVESTIGATOR, Montefiore Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-11-16
Study Completion Date2027-12

Study Record Updates

Study Start Date2022-11-16
Study Completion Date2027-12

Terms related to this study

Additional Relevant MeSH Terms

  • Shock