Status Unknown
A Multicentre, Prospective and Registry Study to Explore the Efficacy and Safety of Mucopolysaccharide Polysulfate Cream in the Treatment of Patients With Eczema
Led by Shenzhen Kangzhe Pharmaceutical Co., Ltd. · Updated on 2022-06-30
1800
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
Sponsors
S
Shenzhen Kangzhe Pharmaceutical Co., Ltd.
Lead Sponsor
B
Beijing Friendship Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
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
Official Title
A Multicentre Study to Explore the Efficacy and Safety of Mucopolysaccharide Polysulfate Cream in Patients With Eczema
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18-75 years of age, male or female;.
- Patients with a clinical diagnosis of subacute or chronic eczema and whose prescription contains Hirudoid®.
- Subjects fully understand the content of this study, sign informed consent.
You will not qualify if you...
- Hypersensitivity to any of the ingredients of this product.
- Patients with heparin hypersensitivity, bleeding-prone constitution and known heparin-induced thrombocytopenia.
- Open wounds and broken skin and mucous membranes
- Patients with localized combined bacterial, viral and fungal infections.
- Pregnant or lactating women or those who are unable to use contraception during the study period
- Those with psychiatric disorders, poor compliance and unable to complete the study.
- Any other reason that the investigator considers inappropriate for inclusion.
Trial Site Locations
Total: 1 location
1
Beijing Friendship Hospital, Capital Medical University
Beijing, Beijing Municipality, China, 100050
Actively Recruiting
Research Team
L
Lingfeng Li
Y
Yue Li
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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