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Completed No phase listed Observational Accepts healthy volunteers

Predictors of Decompressive Laminectomy Outcomes

ClinicalTrials.gov ID: NCT02215551

Public ClinicalTrials.gov record NCT02215551. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 5:13 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Toward Optimizing Decompressive Laminectomy Outcomes: Looking Outside the Spine

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Decompressive laminectomy (DL) is the most common type of back surgery performed in older adults; DL treats lumbar spinal stenosis (LSS), a degenerative narrowing of the spinal canal causes pain and trouble walking. An estimated one in three people who undergo DL do not get well and often undergo repeated surgery.1,3-6 Some studies indicate that conditions outside of the spine (e.g., depression, hip arthritis) cause people who undergo DL to do poorly,27,30-36 but no one has comprehensively examined these conditions or the impact of treating them on DL outcomes. Thus LSS treatment continues to focus on the spine alone.61 The aim of this study is to identify conditions other than LSS that place Veterans at risk of poor DL outcomes so that future comparative effectiveness studies can be designed that examine the impact of a more comprehensive approach to treatment. Investigators believe that a patient-centered rather than a disease-centered approach will lead to superior outcomes, less suffering, and more appropriate use of health care resources.

Study identification

NCT ID
NCT02215551
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
239 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
50 Years to 90 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2014
Primary completion
Jun 30, 2022
Completion
Jan 9, 2023
Last update posted
Jan 11, 2023

2014 – 2023

United States locations

U.S. sites
7
U.S. states
7
U.S. cities
7
Facility City State ZIP Site status
VA Eastern Colorado Health Care System, Denver, CO Denver Colorado 80220
Atlanta VA Medical and Rehab Center, Decatur, GA Decatur Georgia 30033
VA Ann Arbor Healthcare System, Ann Arbor, MI Ann Arbor Michigan 48105
Minneapolis VA Health Care System, Minneapolis, MN Minneapolis Minnesota 55417
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA Pittsburgh Pennsylvania 15240
South Texas Health Care System, San Antonio, TX San Antonio Texas 78229
Hunter Holmes McGuire VA Medical Center, Richmond, VA Richmond Virginia 23249

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02215551, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 11, 2023 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02215551 live on ClinicalTrials.gov.

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