Hospital for Special Surgery
New York, 10021, United States
NCT Number: NCT02300909
Prospective evaluation of the safety and efficacy of dHACM on clinical outcomes in lumbar laminectomy and microdiscectomy patients as assessed by Oswestry Disability Index.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
New York, 10021, United States
The objective of this prospective study is to evaluate the safety and efficacy of dHACM on clinical outcomes in lumbar laminectomy and microdiscectomy patients randomized to one of two groups: 1) without dHACM (control) or 2) dHACM.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Lumbar Decompression Surgery
Microdiscectomy Surgery
Application of Dehydrated Human Amnion/Chorion Membrane (dHACM)
Time frame: 2 years
Patient Functional Outcomes Questionnaire
Time frame: 2 years
Number of patients having re-operation during study
Time frame: 2 years
Dissection of scar formation required at re-operation
Time frame: 2 years
VAS Pain
Time frame: 2 years
SF-36
Time frame: 2 years
HSS Lumbar Expectations Survey
Time frame: 3 months post-op
MiMedx Group, Inc.
Industry
A Randomized, Single Blind, Controlled Trial of Clinical Outcomes of Dehydrated Human Amnion/Chorion Membrane (dHACM) in Lumbar Decompression and Microdiscectomy Surgery
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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