Autologous Adipose-Derived Adult Stromal Vascular Cell Transplantation for Alopecia (A-ADSVC-CT-A)
Primary Purpose
Hair Loss/Baldness, Alopecia
Status
Unknown status
Phase
Not Applicable
Locations
Lebanon
Study Type
Interventional
Intervention
Lipoaspiration
Transplantation
Sponsored by
About this trial
This is an interventional supportive care trial for Hair Loss/Baldness
Eligibility Criteria
Inclusion Criteria:
- Hair loss
- baldness
- alopecia
- Age: ≥ 18 years
- Gender: any
- Willing to collaborate and to attend to the clinical follow-ups for four years
- Patients willing to sign informed consent
- Able and willing to comply with all study requirements
- Patients with no hereditary diseases of the hair, with no burns
- Medically suitable to undergo cell's graft surgery with local anesthesia
- Normal serum chemistry and hematology screening tests
- Negative human immunodeficiency virus (HIV), hepatitis B (HBV), hepatitis C (HCV) serology
- No history of malignancy
- Complete history & physical examination
- Negative chest roentgenogram (CXR)
- Negative urinalysis (U/A)
- Normal thyroid exam
Exclusion Criteria:
- Patients not willing to sign informed consent
- Defects in hair scalp with a potential to affect the graft outcome
- Severe hair loss and baldness
- Infection
- Known allergy
- Known coagulation abnormalities
- Any medical condition likely interferes to cause serious adverse events during the study
- History of malignancy
- History of cognitive impairments or dementia which may impact the patient's ability to participate in the informed consent process and to appropriately complete evaluations
- Any immunodeficiency
- Any current immunosuppressive therapy other than intermittent or low dose corticosteroids
- Renal insufficiency, as defined by creatine level >1.3 mg/dL.
- Serologic evidence of infection with Hepatitis B, Hepatitis C, or HIV
- If female, pregnancy or lactation.
- Any other medical condition, which, in the Investigator's judgment, will interfere with the patient's ability to comply with the protocol, compromises patient safety or interferes with the interpretation of the study results.
Sites / Locations
- Lebanese University, faculty of Sciences, section II and IIIRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
GROUP I
GROUP II
Arm Description
lipoaspiration and transplantation of ADSVCs (for adipose-derived stromal vascular cells/primary fresh cells without culture) Interventions: - Procedure: Lipoaspiration; - Procedure: Transplantation
lipoaspiration and transplantation of ADSCs (for adipose-derived mesynchymal stem cells/after culture) Interventions: - Procedure: Lipoaspiration; - Procedure: Transplantation
Outcomes
Primary Outcome Measures
Improvement of Hair loss
Decrease in the hair loss
Secondary Outcome Measures
Improvement of hair density
Increase in the hair density (Trichometry) from values < 175 hair/ cm² to normal range (175 to 300 hair/ cm²)
Improvement of hair diameter
Increase in the hair diameter from fine hair (≤ 60 microns) to medium hair (60 to 80 microns) and thick hair (≥ 80 microns)
Improvement of the pull test
Decrease in the pull test measures (from 3-8 to 0-1; the number of extracted pulled hairs must be between 0 and 1 in normal patients)
Full Information
NCT ID
NCT03427905
First Posted
January 30, 2018
Last Updated
February 22, 2018
Sponsor
Lebanese University
Collaborators
Reviva Regenerative Medicine Center MEIH Hospital - REVIVA PHARMACEUTICALS (for the first group)
1. Study Identification
Unique Protocol Identification Number
NCT03427905
Brief Title
Autologous Adipose-Derived Adult Stromal Vascular Cell Transplantation for Alopecia
Acronym
A-ADSVC-CT-A
Official Title
Autologous Adipose-Derived Adult Stromal Vascular Cell Transplantation for Alopecia
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 27, 2017 (Actual)
Primary Completion Date
February 3, 2018 (Actual)
Study Completion Date
December 30, 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lebanese University
Collaborators
Reviva Regenerative Medicine Center MEIH Hospital - REVIVA PHARMACEUTICALS (for the first group)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Most common forms of hair loss (alopecia) are caused by aberrant hair follicle cycling and changes in hair follicle morphology. However, current treatments for alopecia do not specifically target these processes. Adipose-derived stromal vascular cells (ADSVCs) that can be harvested from fat cells are one of the latest breakthroughs in the aesthetic field. The potential use of stem cell-based therapies for the repair and regeneration of various tissues and organs offers a paradigm shift that may provide alternative therapeutic solutions. This study aimed at the presentation of clinical cases to suggest a therapeutic plan comprised of acquisition of small volume of fat, followed by injection of ADSVCs in the scalp. 20 patients will be recruited for this study (considering the second group). Hair regeneration will be assessed by the pull test, hair quality, and hair density. All patients must show increased significant improvement of the hair quality and density. The obtained results must prove the efficacy and the safety of the treatment and satisfaction of the patient that will confirm the quality of the results.
Detailed Description
Hair loss is one of the most common complaints among all patients consulting a dermatologist and is usually associated with severe psychological disturbances, distress, and symptoms of depression. Most common forms of hair loss (alopecia) are caused by aberrant hair follicle cycling and changes in hair follicle morphology. Cells with stem cell properties have recently been described in many integument appendages including feathers and teeth, but the hair follicle stands out as one of the best model systems for studying adult stem cells. Hair follicles are accessible, well defined in terms of their developmental biology, and their stem cell populations are located in discrete compartments or niches.
There are three phases of hair growth, which every hair follicle undergoes. The first phase is when follicles undergo extremely rapid epithelial cell division and execute exquisitely timed differentiation programs when in the growing (Anagen) phase. The second phase is when follicles growth stops during a certain period, the (Catagen) phase. The third phase is when most follicles regress into structures that resemble immature developing follicles, after which they go into a period of mitotic quiescence, the (Telogen) phase. Stem cells are at the core of all hair dynamic events that includes a new burst of activity and further morphogenetic remodeling as the follicle grows again at the start of a new Anagen phase.
The term "Stem Cell" is given to a cell which has the ability to self-renew as well as to differentiate into defined cellular subtypes. Multipotent stem cells are present in different adult tissues such as bone marrow, dental pulp, adipose tissue, etc. and within the adipose tissue the adipose-derived stromal vascular cells (ADSVCs), which are one of the most promising stem cell population identified since the human adipose tissue is easily obtained in large quantities with little patient discomfort and secretory factors from ADSVCs have been considered as a promising therapy for skin aging. Therefore, the use of autologous ADSVCs can be promising for hair loss. Since the stromal vascular fraction (SVF) is saturated with stem cells among other cells derived from adipose tissue, cells can be called ADSVFC if they are used freshly, or ADSC/ADASC or others terms in cases of primary cells placed in culture having then the adherent feature, resulting in a set of mesenchymal stem cells (MSCs). In fact, contrary to cultured ADSCs, freshly isolated ADSVCs were shown to be highly positive for CD34, and positive for CD117 and HLA-DR. MSCs derived from adipose tissue when obtained by culture are mostly negative for CD34, and HLA-DR. This indicates clearly that primary cells are significantly more promising in cases of need to maintain a certain level of CD34 in the graft.
In the present study, the investigators aimed to use autologous ADSVCs graft for the treatment of alopecia and to assess the safety and effectiveness of the transplantation. This ADSVCs group will be compared to a group of cultured ADSCs. In fact, the study is divided into 2 groups: ADCVCs and ADSCs, where the first group had been started in 2013 and since 2016, the investigators aimed to add a comparative group by using the cultured ADSCs instead of the primary non-cultured ADSVCs. (Note: the investigators started using grafts of PRP (Platelets Rich Plasma) in 2013 before using isolated adipose-derived cells, where no significant improvement in the hair quality was observed. Then, the investigators aimed to use adipose-derived cells firstly without culture and secondly subjected to culture. The first group was done in collaboration with Reviva Regenerative Medicine Center at the Middle East Institute of Health University Hospital at Bsalim Lebanon. The second group will be realized with a collaborator to be defined by the Lebanese University after approval of the administration and corresponding committee.
The process flow is defined as following: (1) the file study: which start by receiving the file of the patient, the file will be forwarded to appointed physician coordinator for review and submission of medical report (Here Dr. Rami Anderi), then the medical report will be evaluated by the cell therapy committee and the patient will be asked for clinical examination, and after consultation a reply to the patient with medical decision will follow with an approval or not be recruited and if yes, a brief report about the procedure will be submitted and explained in details to the patient, a consent form must be signed if the patient agrees to be included in the study, (2) the patient admission: which may start by completion of the procedure forms and doing the pre-op evaluation (initial work up defined as a clinical and biological assessment upon C.A.S), followed by lipoaspiration of the subcutaneous adipose tissue to be performed by the plastic surgeon, then sample processing for isolation and characterization of the stromal vascular fraction enriched with ADSVCs (the quality control assessment will be realized before and after all the steps of the procedure starting from the SVF collection to transplantation; (3) the delivery (transplantation). The patient will be put on antibiotic/anti-inflammatory for a defined period and followed by the team at 1 week, 3 months, and 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hair Loss/Baldness, Alopecia
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
GROUP I
Arm Type
Active Comparator
Arm Description
lipoaspiration and transplantation of ADSVCs (for adipose-derived stromal vascular cells/primary fresh cells without culture) Interventions: - Procedure: Lipoaspiration; - Procedure: Transplantation
Arm Title
GROUP II
Arm Type
Active Comparator
Arm Description
lipoaspiration and transplantation of ADSCs (for adipose-derived mesynchymal stem cells/after culture) Interventions: - Procedure: Lipoaspiration; - Procedure: Transplantation
Intervention Type
Procedure
Intervention Name(s)
Lipoaspiration
Intervention Description
Procedure: Lipoaspiration of fat and processing for the isolation of SVF Procedure: Transplantation
Intervention Type
Procedure
Intervention Name(s)
Transplantation
Intervention Description
Procedure: Lipoaspiration of fat and processing for the isolation of SVF and culture for the obtention of ADSCS Procedure: Transplantation
Primary Outcome Measure Information:
Title
Improvement of Hair loss
Description
Decrease in the hair loss
Time Frame
6 months postoperative
Secondary Outcome Measure Information:
Title
Improvement of hair density
Description
Increase in the hair density (Trichometry) from values < 175 hair/ cm² to normal range (175 to 300 hair/ cm²)
Time Frame
6 months postoperative
Title
Improvement of hair diameter
Description
Increase in the hair diameter from fine hair (≤ 60 microns) to medium hair (60 to 80 microns) and thick hair (≥ 80 microns)
Time Frame
6 months postoperative
Title
Improvement of the pull test
Description
Decrease in the pull test measures (from 3-8 to 0-1; the number of extracted pulled hairs must be between 0 and 1 in normal patients)
Time Frame
6 months postoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Hair loss
baldness
alopecia
Age: ≥ 18 years
Gender: any
Willing to collaborate and to attend to the clinical follow-ups for four years
Patients willing to sign informed consent
Able and willing to comply with all study requirements
Patients with no hereditary diseases of the hair, with no burns
Medically suitable to undergo cell's graft surgery with local anesthesia
Normal serum chemistry and hematology screening tests
Negative human immunodeficiency virus (HIV), hepatitis B (HBV), hepatitis C (HCV) serology
No history of malignancy
Complete history & physical examination
Negative chest roentgenogram (CXR)
Negative urinalysis (U/A)
Normal thyroid exam
Exclusion Criteria:
Patients not willing to sign informed consent
Defects in hair scalp with a potential to affect the graft outcome
Severe hair loss and baldness
Infection
Known allergy
Known coagulation abnormalities
Any medical condition likely interferes to cause serious adverse events during the study
History of malignancy
History of cognitive impairments or dementia which may impact the patient's ability to participate in the informed consent process and to appropriately complete evaluations
Any immunodeficiency
Any current immunosuppressive therapy other than intermittent or low dose corticosteroids
Renal insufficiency, as defined by creatine level >1.3 mg/dL.
Serologic evidence of infection with Hepatitis B, Hepatitis C, or HIV
If female, pregnancy or lactation.
Any other medical condition, which, in the Investigator's judgment, will interfere with the patient's ability to comply with the protocol, compromises patient safety or interferes with the interpretation of the study results.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nehman A. Makdissy, PhD
Phone
0096171210250
Email
almakdissy@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rami Anderi, MD
Phone
0096895919143
Email
cosmeclic@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nehman Makdissy, PhD
Organizational Affiliation
Lebanese University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rami Anderi, MD
Organizational Affiliation
Lebanese University
Official's Role
Study Director
Facility Information:
Facility Name
Lebanese University, faculty of Sciences, section II and III
City
Beirut
ZIP/Postal Code
99
Country
Lebanon
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nehman Makdissy
Phone
0096171210250
Email
almakdissy@hotmail.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Autologous Adipose-Derived Adult Stromal Vascular Cell Transplantation for Alopecia
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