A Multicentre Study to Explore the Efficacy and Safety of Mucopolysaccharide Polysulfate Cream in Patients With Eczema
NCT05439577 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1800
Last updated 2022-06-30
Summary
The study was designed to collect information over 1800 patients with a clinical diagnosis of subacute or chronic eczema, these patients' prescriptions contain Hirudoid®. EASI, IGA and more indicators are evaluated. Data were collected for a maximum of 12 weeks according to the clinician's consultation and follow-up (Time points were set at baseline, 1, 2, 3, 4, 8 and 12 weekends). The above data were analysed to explore the optimal treatment modality, dose and treatment period for patients with subacute or chronic eczema.
Conditions
Interventions
- DRUG
-
Mucopolysaccharide Polysulfate Cream
Patients using Hirudoid® alone
- DRUG
-
Mucopolysaccharide Polysulfate Cream and glucocorticoids
Patients using Hirudoid® and glucocorticoids (Combination therapy, but not always)
Sponsors & Collaborators
-
Beijing Friendship Hospital
collaborator OTHER -
LanZhou University
collaborator OTHER -
The First Hospital of Hebei Medical University
collaborator OTHER -
Xingtai People's Hospital
collaborator OTHER -
Beijing Boai Hospital
collaborator OTHER -
Guangxi Ruikang Hospital
collaborator OTHER -
The Third Affiliated Hospital of Southern Medical University
collaborator OTHER_GOV -
The Second Affiliated Hospital of Jiaxing University
collaborator OTHER -
Wuxi People's Hospital
collaborator OTHER -
Shenzhen Kangzhe Pharmaceutical Co., Ltd.
lead INDUSTRY
Principal Investigators
-
Lingfeng Li · Beijing Friendship Hospital
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-09-23
- Primary Completion
- 2022-09-30
- Completion
- 2022-11-30
Countries
- China
Study Locations
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