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Xia Shi Surgical Treatment for Eczema Multi-center Clinical Research

Phase 2
Conditions
Eczema
Interventions
Drug: Furoic acid loperamide hydrochloride cream
Drug: Mullite ointment
Drug: 3% boric acid solution
Drug: Zine oxide
Registration Number
NCT02517957
Lead Sponsor
Shanghai Yueyang Integrated Medicine Hospital
Brief Summary

On the basis of Xiashi skin surgery clinical experience, this project adopts the multicenter, randomized, double-blind, controlled trial of design type. Objective, normative evaluation of traditional Chinese medicine cool blood latent town effectiveness of therapeutic regimen in the treatment of eczema, security, and control of the relapse of situation, provide high-level evidence-based basis for traditional Chinese medicine treatment of eczema, aims to form suitable for popularization and application of traditional Chinese medicine in the treatment of eczema.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
342
Inclusion Criteria
  • accord with standard of syndrome differentiation of traditional Chinese medicine (blood hot sheng) and western medicine diagnostic criteria (subacute eczema);
  • age between 18-65 years old, gender, ethnic unlimited;
  • agreed to participate in clinical trials can observe and cooperate with the visitor on schedule;
  • volunteered for this study and obtain informed consent will be;
  • lesion area of about 5-30% of surface area (BSA) were (containing 3% and 3%, palm measurement method)
  • IGA scale of 1 to 3 points (including);
  • her lesions mainly located in the trunk and limbs (or);
  • Women HCG negative;
Exclusion Criteria
  • known to the study of drug allergy to any of the components;
  • previous or current with any may affect the results of systemic disease, or other activity of skin diseases (such as: psoriasis);
  • has a liver and kidney function is not complete, liver damage of ALT and AST > 1.5 times the upper limit of normal, renal BUN > 1.5 times the upper limit of normal or creatinine > 1.5 times the upper limit of normal value;
  • QTcB or QTcF acuity 450 milliseconds. For subjects QTc acuity bundle branch block 480 milliseconds.
  • prior or current with clinical significance of cardiovascular, lung disease, gastrointestinal tract, liver, kidney, blood, nerve abnormalities or mental disease;
  • breast-feeding or plan to pregnant women during test;
  • skin area score > 30%;
  • eosinophil count score > 10%
  • for nearly two weeks taking corticosteroids or a week, both inside and outside with corticosteroid preparation;
  • three months received study medication or other participated in other clinical subjects;
  • for any reason cannot cooperate research, for example: how language understanding, not to research centers, etc.;
  • Researchers believe can bring obvious risk patients or confuse the results of the study, which should rule out other conditions or disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Qinzhuliangxue Keli3% boric acid solutionQinzhuliangxue Keli(common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets placebo (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.)
loratadine tabletsFuroic acid loperamide hydrochloride creamQinzhuliangxue Keli placebo (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.),Loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
Qinzhuliangxue and loratadineFuroic acid loperamide hydrochloride creamQinzhuliangxue Keli (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
Qinzhuliangxue and loratadine3% boric acid solutionQinzhuliangxue Keli (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
Qinzhuliangxue KeliFuroic acid loperamide hydrochloride creamQinzhuliangxue Keli(common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets placebo (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.)
Qinzhuliangxue and loratadineMullite ointmentQinzhuliangxue Keli (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
Qinzhuliangxue KeliMullite ointmentQinzhuliangxue Keli(common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets placebo (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.)
Qinzhuliangxue KeliZine oxideQinzhuliangxue Keli(common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets placebo (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.)
loratadine tablets3% boric acid solutionQinzhuliangxue Keli placebo (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.),Loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
loratadine tabletsZine oxideQinzhuliangxue Keli placebo (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.),Loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
Qinzhuliangxue and loratadineZine oxideQinzhuliangxue Keli (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.), loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
loratadine tabletsMullite ointmentQinzhuliangxue Keli placebo (common name: QZLX particles, shenzhen China resources san-jiu pharmaceutical trading co., LTD.),Loratadine tablets (common name: LLTD piece, Shanghai schering pharmaceutical co., LTD.).
Primary Outcome Measures
NameTimeMethod
Change from Baseline in the Eczema Area and Severity Index (EASI) scoreBaseline and up to week 4 of the follow up phase
Secondary Outcome Measures
NameTimeMethod
Change in Itching degree scoreBaseline and up to week 4 of the follow up phase
Dermatology life quality index (DLQI)Baseline and up to week 4 of the follow up phase
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