Multiple Sclerosis Clinical Trial

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Safety and Clinical Outcomes Study: SVF Deployment for Orthopedic, Neurologic, Urologic, and Cardio-pulmonary Conditions

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Summary

To evaluate for any adverse effects that may be related to the administration and reception of autologous adipose derived stromal vascular fraction (SVF). Secondarily, the study monitors the results of subjective and objective findings as it applies to the non-blinded deployment of autologous SVF for various inflammatory and/or degenerative conditions including select orthopedic, neurologic, urologic and cardio-pulmonary conditions. SVF deployments include intra-venous, intra-articular, and soft tissue injections.

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Full Description

SVF Stromal Vascular Fraction is obtained by lipoharvesting, procurement, and lipo-transfer as a same day operative procedure

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Eligibility Criteria

Inclusion Criteria

Patient must be age 16 or older
Patient must have a degenerative disease or inflammatory disease that meets criteria for treatment under the IRB which includes: Arthritis, Auto-immune disease,COPD, Cardiomyopathy, Peyronies Disease,Interstitial Cystitis, Erectile Dysfunction, and Neurodegenerative disease such as Parkinsons, ALS, Neuropathy.
Patient must be healthy enough to tolerate a local anesthetic

Exclusion Criteria:

Patient must not have active cancer
Patient must not have active infection

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

3000

Study ID:

NCT01953523

Recruitment Status:

Completed

Sponsor:

Elliot Lander

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There is 1 Location for this study

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California Stem Cell Treatment Center
Rancho Mirage California, 92270, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

3000

Study ID:

NCT01953523

Recruitment Status:

Completed

Sponsor:


Elliot Lander

How clear is this clinincal trial information?

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