Xiaoning Yan

Dr. Xiaoning Yan


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2021 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
XLXiao Qiang Li
Xiao Qiang Li
YCYong Chen
Yong Chen
GDGuan Cheng Dai
Guan Cheng Dai
BZBei Bei Zhou
Bei Bei Zhou
XYXiaoning Yan
Xiaoning Yan
Ren Xiang TanRen Xiang Tan
Ren Xiang Tan

17 June 2021 in Molecular Genetics and Genomics
Verified
Journal Article
Closed access
PDF file
YLYing Luo
Ying Luo
KQKeshen Qu
Keshen Qu
LKLe Kuai
Le Kuai
YRYi Ru
Yi Ru
KHKeke Huang
Keke Huang
MXMeng Xing
Meng Xing

25 August 2020 in Trials
Verified
Journal Article
Open access
PDF file
LLLiu Liu
Liu Liu
YLYi Lu
Yi Lu
XYXiaoning Yan
Xiaoning Yan
SYSuqing Yang
Suqing Yang
LGLi-Ping Gong
Li-Ping Gong
BLBin Li
Bin Li
Background: Fire needle therapy is a characteristic treatment in traditional Chinese medicine (TCM). An increasing number of studies have indicated that fire needle treatment for psoriasis provides satisfactory results with few side effects and a low recurrence rate. We herein describe the protocol for a multicenter, randomized, single-blind, placebo-controlled trial that will provide high-quality evidence on the efficacy and safety of fire needle therapy for plaque psoriasis. Methods: Ninety-two patients with blood stasis syndrome (BSS) of plaque psoriasis will be enrolled and randomly assigned to receive fire needle therapy (intervention group) or fire needle control therapy (control group) once a week for 4 weeks. The Psoriasis Area and Severity Index (PASI) score will serve as the major efficacy index, while the body surface area (BSA), Physician Global Assessment (PGA) score, Dermatology Life Quality Index (DLQI) score, patient-reported quality of life (PRQoL), visual analog scale (VAS) score for itching, TCM symptom score, and relapse rate will be assessed as secondary outcomes. The PASI score, BSA, PGA score, and VAS score for itching will be evaluated at baseline and during the 4-week treatment and follow-up periods. DLQI score, PRQoL, and TCM symptom score will be assessed at baseline and during the treatment period. Recurrence will be evaluated during the follow-up period. Safety assessments include vital sign monitoring, routine blood tests, blood biochemistry, routine urine tests, pregnancy tests, physical examinations, and adverse-event recording. SAS software will be used for data analysis. The data network platform will be designed by the data management center of Nanjing Ningqi Medical Technology Co., Ltd. Discussion: It is believed that fire needle therapy can activate the meridians, promote blood circulation, and regulate skin immunity. BSS of plaque psoriasis is related to not only immune dysfunction but also poor or stagnant blood flow. We anticipate that the results of the trial described in this protocol will provide strong evidence for the safety and efficacy of fire needle therapy for BSS of plaque psoriasis. Trial registration: Clinicaltrials.gov NCT03953885. Registered on May 15, 2019. Name: Fire Needle Therapy on Plaque Psoriasis with Blood Stasis Syndrome

1 October 2019 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
XLXiao Qiang Li
Xiao Qiang Li
YCYong Chen
Yong Chen
HZHong Mei Zhou
Hong Mei Zhou
HSHui Li Shi
Hui Li Shi
XYXiaoning Yan
Xiaoning Yan
Ren Xiang TanRen Xiang Tan
Ren Xiang Tan

1 June 2021 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
KQKe-Shen Qu
Ke-Shen Qu
YLYing Luo
Ying Luo
XYXiaoning Yan
Xiaoning Yan
KLKuai Le
Kuai Le
YRYi Ru
Yi Ru
MXMeng Xing
Meng Xing

26 February 2020 in Trials
Verified
Journal Article
Open access
PDF file
MXMeng Xing
Meng Xing
XYXiaoning Yan
Xiaoning Yan
SYSuqing Yang
Suqing Yang
LLLinge Li
Linge Li
LGLiping Gong
Liping Gong
XLXin Li
Xin Li
Background: It is difficult to achieve a balance among safety, efficacy, and cost for the clinical treatment of plaque psoriasis. The current treatment of psoriasis often involves comprehensive therapy such as topical plasters, internal medicine, and phototherapy, which are expensive, and some of the drugs have serious side effects. Moving cupping is a type of cupping that has been used clinically for thousands of years in China. It has the advantage of being inexpensive and easy to perform. Therefore, it is widely used in public hospitals in China for psoriasis treatment. However, a comprehensive evaluation of the current clinical evidence of its efficacy is lacking. In this study, we aimed to evaluate the efficacy and safety of moving cupping to treat plaque psoriasis. Methods: A multicenter, two-arm parallel group, single-blind, randomized, controlled trial will be conducted at six hospitals in China between August 1, 2019 and December 31, 2021. A total of 122 adult patients (aged 18–65 years) who meet the inclusion criteria are being recruited. Participants will receive either basic treatment combined with moving cupping therapy or basic treatment combined with moving cupping placebo. The treatment cycle will be 4 weeks, and the efficacy of treatment will be assessed weekly by the Psoriasis Area and Severity Index during the treatment period and follow-up visits at weeks 6 and 8. The body surface area, physician’s global assessment, Dermatology Life Quality Index, patient-reported quality of life, visual analog scale, Traditional Chinese Medication syndrome scoring scale, combined medication, and adverse events will also be recorded and compared to the relative baseline values. Discussion: The findings of this trial may lead to better decisions regarding the treatment of plaque psoriasis. If the trial outcomes are considered favorable, this ancient Chinese medical therapy may be worthy of widespread use because of its convenience and low cost. Trial registration: This study was registered on May 15,2019 at ClinicalTrials.gov with the identifier number NCT03952676.