RECRUITING

Outcomes for Lumbar Decompressions With Use of Liposomal Bupivicaine

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

Evaluate the benefit of using liposomal bupivicaine in lumbar laminectomies in terms of length of stay, IV narcotic use, 30-day narcotic use, visual analog score (VAS) and 30-day readmissions

Official Title

A Double Blinded Randomized Control Trial in Outcomes for Lumbar Decompressions With Use of Liposomal Bupivicaine

Quick Facts

Study Start:2019-09-08
Study Completion:2025-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04066296

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. 1. Male or Female
  2. 2. Adult (≥18 yo)
  3. 3. Lumbar stenosis
  1. 1. Co-morbidities precluding surgery
  2. 2. ≤18 yo
  3. 3. Pregnant
  4. 4. Breastfeeding
  5. 5. Need for instrumented fusion
  6. 6. Prisoners
  7. 7. Intra-operative CSF leak (identified by gush of CSF)
  8. 8. Daily pre-operative opioid use of \> 25 morphine Eq/day
  9. 9. Previous lumbar surgery at indicated level

Contacts and Locations

Study Contact

Jens-Peter Witt, MD, PhD
CONTACT
303-724-2306
peter.witt@cuanschutz.edu
Akal Sethi, MD
CONTACT
303-724-1995
akal.sethi@cuanschutz.edu

Study Locations (Sites)

University of Colorado Anschutz Medical Campus
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

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 Date2019-09-08
Study Completion Date2025-01

Study Record Updates

Study Start Date2019-09-08
Study Completion Date2025-01

Terms related to this study

Additional Relevant MeSH Terms

  • Lumbar Spinal Stenosis