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Alopecia clinical trials

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NCT ID: NCT03388840 Recruiting - Clinical trials for Androgenetic Alopecia

Adipose Derived Stem Cells Versus Platelet Rich Plasma on Follicular Unit Extraction

Start date: January 15, 2018
Phase: Phase 4
Study type: Interventional

Androgenetic alopecia is the most common type of alopecia in both men and women. About 80 % of Caucasian men and 40-50 % of Caucasian women are affected by androgenetic alopecia. The psychological impact of hair loss due to Androgenetic alopecia can be profound.

NCT ID: NCT03248193 Recruiting - Clinical trials for Chemotherapy-induced Peripheral Neuropathy (CIPN)

Concomitant Limb Cryocompression and Scalp Cooling to Reduce Paclitaxel-induced Neuropathy and Alopecia

Start date: August 4, 2017
Phase: N/A
Study type: Interventional

Paclitaxel is a chemotherapy drug that is used to treat breast cancer, one of the most common cancers. It causes two side effects very often - hair-loss and numbness. Until recently, there have been no known ways to prevent or treat either side effect. Recently, cooling of the scalp to prevent hair loss caused by paclitaxel was approved. Our team is developing a method to prevent numbness caused by paclitaxel by using a device that cools the arms and the legs, while applying mild pressure, and this technique is called cryocompression. As scalp cooling use in day-to-day cancer care increases, future studies involving cryocompression to treat neuropathy must take this into account, lest patients be denied or are required to trade-off one treatment for the other. However, there is concern of causing a reduction in core body temperature, which would not be safe or a general intolerance to this treatment. Both scalp cooling and limb cryocompression individually have not shown to cause this, but simultaneous use has not been studied previously. Clinical safety studies, in healthy subjects and cancer patients would need to be conducted to prove this theory, which is being proposed by currently.

NCT ID: NCT03078686 Recruiting - Alopecia Areata Clinical Trials

Biocellular-Cellular Regenerative Treatment Scaring Alopecia and Alopecia Areata

SAAA
Start date: February 17, 2017
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the safety and efficacy of the use of a biocellular mixture of emulsified adipose-derived tissue stromal vascular fraction (AD-tSVF) and high density platelet-rich plasma concentrate (HD- PRP). Additionally, comparison with clinical outcomes of adipose-derived cellular Stromal Vascular Fraction (AD-cSVF) + AD-tSVF + HD PRP; AD-cSVF + emulsified AD-tSVF + HD- PRP; emulsified AD-tSVF + HD PRP + AD-cSVF; AD-cSVF via intravenous infusion in treatment of Scaring Alopecias and Alopecia Areata. Control will be served by use of established clinical protocol of using platelet concentrates with Matristem Matrix (Acel) injected in the same fashion as the other ARMs within this study, and comparative analyses performed at the endpoint of this study.

NCT ID: NCT02856308 Recruiting - Alopecia Clinical Trials

Hairstetics Hair Implant Device Safety and Efficacy

Start date: March 2014
Phase: N/A
Study type: Interventional

This is a prospective, single-arm, multi-center, international, open-label, non-randomized, clinical study. The aim of the study is to assess the safety and efficacy of the use of the Hairstetics hair implant device in subjects affected with hair loss.

NCT ID: NCT02797223 Recruiting - Clinical trials for Chemotherapy-induced Alopecia

"Impact of Chemotherapy-induced Alopecia on the Quality of Life of Women With Breast Cancer"

Start date: June 2016
Phase: N/A
Study type: Observational

The main objective of this qualitative phenomenological study is to understand the impact of chemotherapy-induced alopecia, the quality of life of women with breast cancer from this experience. The study will be conducted in the day hospital oncology-hematology of the Hospital de la Santa Creu i Sant Pau. Data collection will be done through semi-structured interviews. About 12 to 14 interviews throughout the study was conducted. So in the study involved a total of between 12 and 14 women. These will be recorded in voice and then transcribe and code. From reading and re-reading the patterns or data that relate to each other, thus establishing the categories (thematic analysis) were identified. These categories describe the experiences of the participants alopecia.

NCT ID: NCT02604888 Recruiting - Alopecia Areata Clinical Trials

Efficacy Study of a Cosmetic Lotion in the Treatment of Alopecia Areata in Males and Females

MEXISAREATA
Start date: October 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the Hair Loss Prevention Lotion named MEXIS, M.P.A.F., M6S PATENT is effective in the treatment of Alopecia Areata.

NCT ID: NCT02591823 Recruiting - Clinical trials for Rheumatoid Arthritis

Hair Fall in Patients on Low Dose Methotrexate

Start date: October 2015
Phase: N/A
Study type: Observational

Low dose methotrexate used in rheumatoid arthritis is considered very safe and has a side effect profile very different from that seen with high dose methotrexate used in oncology. Hair fall has been found to occur in high dose methotrexate but there is no data regarding the same when methotrexate is used in low dose.Thus this observational case control study is being undertaken to determine whether rheumatoid arthritis patients really need to be concerned about hair fall when on low dose methotrexate.

NCT ID: NCT02154503 Recruiting - Clinical trials for Androgenetic Alopecia

Evaluating the Efficacy of Microneedling in the Treatment of Androgenetic Alopecia

Start date: April 2014
Phase: Phase 1
Study type: Interventional

Androgenetic Alopecia is the most common non scarring alopecia worldwide. Treatment of which has been limited with few options for medical and surgical treatment, the cost of the latter being prohibitive for many. Recently there have been several new modalities proposed as treatment, namely Microneedling and Platelet Rich Plasma. Microneedling has been shown to overexpress hair growth factors which may enhance or stimulate miniaturized hairs to grow. It has also been shown to increase the absorption of topical products significantly. The exact mechanism of action of Microneedling is still being delineated. In this study, we aim to do a half lesional study with global photographs and hair counts done at the start of , week four and week twelve. Patients would be needled once weekly after application of topical anaesthetic (5% EMLA). If by week six there is significant regrowth (>30%), then total lesional needling will be done. Patients will only be using topical 5% Minoxidil throughout the study as this will prolong the effects of the regrowth.

NCT ID: NCT02074943 Recruiting - Clinical trials for Androgenetic Alopecia

Efficacy and Safety of Platelet Rich Plasma in Androgenetic Alopecia

Start date: April 2014
Phase: N/A
Study type: Interventional

The investigators plan to conduct a clinical trial to assess the effects and safety of platelet rich plasma on androgenetic alopecia.

NCT ID: NCT01802177 Recruiting - Alopecia Areata Clinical Trials

Excimer Light for Alopecia Areata

Start date: February 2013
Phase: Phase 2
Study type: Interventional

Alopecia Areata (AA) is a chronic autoimmune inflammatory disease causing nonscarring hair loss. Many treatment modalities have been found to be helpful in AA, however, none on them cure the disease. UVB excimer light has recently emerged as a new therapeutic modality in many dermatologic diseases. There are no prospective randomized controlled trials evaluating the efficacy and safety of UVB excimer light in AA. We plan on conducting a prospective split lesion single-blinded randomized clinical trial to assess efficacy and safety of UVB excimer light in the treatment of AA.