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DC Field | Value | Language |
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dc.contributor.author | Thianboonsong T. | |
dc.contributor.author | Kanokrungsee S. | |
dc.contributor.author | Paichitrojjana A. | |
dc.contributor.author | Udompataikul M. | |
dc.contributor.author | Kamanamool N. | |
dc.contributor.author | Rojhirunsakool S. | |
dc.date.accessioned | 2021-04-05T03:05:24Z | - |
dc.date.available | 2021-04-05T03:05:24Z | - |
dc.date.issued | 2020 | |
dc.identifier.issn | 13960296 | |
dc.identifier.other | 2-s2.0-85092284609 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/12732 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85092284609&doi=10.1111%2fdth.14354&partnerID=40&md5=a28dcd44bf2325cb63658e0cc502d497 | |
dc.description.abstract | This study evaluated the efficacy and tolerability of topical aluminum sesquichlorohydrate (AS) when compared to aluminum chloride (AC) as a treatment for primary axillary hyperhidrosis (PAH). Twenty subjects were included in this randomized, controlled, split-side 8-week study. All participants applied 20% AS and 20% AC lotions in their axillae (one treatment per axilla) every night for 2 weeks; next, the application was reduced to three times a week for 4 weeks. The assessment was performed using the sweating intensity visual scale (SIVS), hyperhidrosis disease severity score (HDSS), patient satisfaction score, and the appearance of adverse effects on weeks 0, 1, 2, 4, 6, and 8. Both AS as well as AC application showed positive results, significantly differing from the baseline, as assessed using SIVS, HDSS, and patient satisfaction score at every follow-up visit; however, no significant difference was observed between the AS and AC groups at any follow-up visit. The mean time of response was 1.14 weeks for both treatments. A side effect was observed in one subject (5%), who reported itching on the AC axilla. The therapeutic effects persisted even after reducing the frequency of application and lasted for at least 2 weeks after cessation of use. In conclusion, topical 20% AS demonstrated similar efficacy to topical 20% AC in the treatment of PAH, with a high safety profile. © 2020 Wiley Periodicals LLC. | |
dc.rights | Srinakharinwirot University | |
dc.subject | aluminum chloride | |
dc.subject | aluminum salt | |
dc.subject | aluminum sesquichlorohydrate | |
dc.subject | antiperspirant agent | |
dc.subject | non prescription drug | |
dc.subject | unclassified drug | |
dc.subject | adult | |
dc.subject | Article | |
dc.subject | axilla | |
dc.subject | clinical article | |
dc.subject | clinical evaluation | |
dc.subject | clinical observation | |
dc.subject | comparative effectiveness | |
dc.subject | controlled study | |
dc.subject | disease severity assessment | |
dc.subject | double blind procedure | |
dc.subject | drug efficacy | |
dc.subject | drug safety | |
dc.subject | drug tolerability | |
dc.subject | female | |
dc.subject | follow up | |
dc.subject | human | |
dc.subject | hyperhidrosis | |
dc.subject | hyperhidrosis disease severity score | |
dc.subject | lotion | |
dc.subject | low level laser therapy | |
dc.subject | male | |
dc.subject | night | |
dc.subject | patient satisfaction | |
dc.subject | prospective study | |
dc.subject | pruritus | |
dc.subject | randomized controlled trial | |
dc.subject | skin disease assessment | |
dc.subject | sweating intensity visual scale | |
dc.subject | therapy effect | |
dc.subject | topical treatment | |
dc.subject | treatment response | |
dc.title | Efficacy and tolerability of 20% aluminum sesquichlorohydrate vs 20% aluminum chloride for the treatment of axillary hyperhidrosis: A randomized controlled trial | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Dermatologic Therapy. Vol 33, No.6 (2020) | |
dc.identifier.doi | 10.1111/dth.14354 | |
Appears in Collections: | Scopus 1983-2021 |
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