Autopsy report · NCT03797144
Fenestrated Screw Study
Cause of deathStaffing, sites or logistics
“Delay in enrollment as compared to plan (impacted by COVID-19 pandemic) and availability of data from other data sources to support the products in scope.”
Life of this trial
- Registered 4 months before it started.
- Ran for about 1 year 3 months before it stopped.
- 27 participants enrolled.
- Results were posted on the registry 1 year 1 month after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Medtronic Spinal and Biologics
- Sponsor type
- Industry
- Conditions
- Degenerative Spinal Disease; Deformity of Spine
- Interventions
- CD HORIZON® Fenestrated Screw System with Fenestrated Screw Cement
- Participants
- 27
- Sites
- 6
- Countries
- Belgium, Finland, France, Greece, Italy
Trials that died the same way
- Oxidative Stress and Circulating Nuclear DNA (cfDNA) in Acute Kidney Injury and Continuous Renal Replacement Therapies.
“Enrollment slower than anticipated and interrupted by COVID-19 pandemic” - Quality of Life Changes on Lower Extremity Lymphedema Patients Using an Advanced Pneumatic Compression Device (PCD)
“Due to slow enrollment during COVID” - Pro-permeability and Pro-fibrosis Factors in the Aqueous of Patients With Retinal Diseases
“Enrollment was affected due to the COVID-19 pandemic” - Study of Latiglutenase in T1D/CD Patients
“Covid-19 interruptions and enrollment challenges” - Impact of App Based Diabetes Training Program in Conjunction With the BD Nano Pen Needle in People With T2 Diabetes
“Enrollment halted prematurely due to the Covid-19 pandemic”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.