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Study identifier: NCT04042844 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD)

Condition: Lumbar Disc Disease  ·  Sponsor: BioRestorative Therapies

PhasePhase 2
Planned participants99
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a double-blind, controlled, randomized study with blinded assessments using a single dose. Subjects that have a current diagnosis of chronic lumbar disc disease and meet eligibility criteria will be enrolled. Chronic lumbar disc disease is defined as back and/or radicular pain with degeneration of the disc confirmed by patient history, physical examination, and radiographic measures such as computed tomography (CT), magnetic resonance imaging (MRI), plain film, myelography, discography, or other acceptable means.

This description comes directly from the study's public registry record.

Talk to the study team

Francisco Silva  ·  1(949)394-0132  ·  FSilva@biorestorative.com

Always discuss trial participation with your own doctor first.

Locations (19)

Alabama Clinical Therapeutics, LLCBirmingham, Alabama, United StatesWithdrawn
Source HealthcareSanta Monica, California, United StatesRecruiting
Boomerang HealthcareWalnut Creek, California, United StatesRecruiting
Denver Back Pain Specialists, LLCGreenwood Village, Colorado, United StatesRecruiting
Cantor Spine InstituteFort Lauderdale, Florida, United StatesWithdrawn
Coastal HealthJacksonville, Florida, United StatesRecruiting
Pain Relief CentersSt. Petersburg, Florida, United StatesRecruiting
Tampa Pain Relief CenterTampa, Florida, United StatesRecruiting
Florida Pain Relief CenterTampa, Florida, United StatesRecruiting
Conquest ResearchWinter Park, Florida, United StatesRecruiting
Northwell HealthNew York, New York, United StatesRecruiting
The Center of Clinical Research, LLCWinston-Salem, North Carolina, United StatesRecruiting

+ 7 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT04042844