The Use of Exosomes In Craniofacial Neuralgia
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Conditions studied: Neuralgia
In brief
This study is designed to evaluate the safety and efficacy of exosome deployment in patients with Craniofacial Neuralgia. Secondarily, this study is designed to rigorously evaluate for any adverse events that may be related to the administration and reception of exosomes.
Key facts
- Study ID
- NCT04202783
- Run by
- Neurological Associates of West Los Angeles
- People needed
- 100
- Starts
- 2023-12-01
- Expected to finish
- 2024-12-01
- Last updated by the study team
- 2022-09-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or Female at least 18 years of age
- Clinical diagnosis of craniofacial neuralgia
You may not qualify if…
- Subjects unable to give informed consent
- Subjects who would not be able to lay down without excessive movement in a calm environment sufficiently long enough to be able to achieve sleep
- Recent surgery or dental work within 3 months of the scheduled procedure.
- Pregnancy, women who may become pregnant or are breastfeeding
- Advanced terminal illness
- Any active cancer or chemotherapy
- Bone marrow disorder
- Myeloproliferative disorder
- Sickle cell disease
- Primary pulmonary hypertension
- Immunocompromising conditions and/or immunosuppressive therapies
- Macular degeneration
- Subjects with scalp rash or open wounds on the scalp (for example from treatment of squamous cell cancer)
- Advanced kidney, pulmonary, cardiac or liver failure
- Subjects with vascular causes of dementia
- Bleeding disorder, untreated
Where it is running
- Neurological Associates of West LA — Santa Monica, California, United States
Full record on ClinicalTrials.gov
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