Efficacy and Safety of AD-MSCs Plus Calpocitriol Ointment in Patients With Moderate to Severe Psoriasis
Launched by GUANGDONG PROVINCIAL HOSPITAL OF TRADITIONAL CHINESE MEDICINE · Jan 4, 2018
Trial Information
Current as of May 14, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. moderate to severe psoriasis vulgaris ( PASI \> 10 or BSA \>10%)
- • 2. 18 to 65 years old
- • 3. written/signed informed consent
- Exclusion Criteria:
- • 1. guttate psoriasis, inverse psoriasis or exclusively associated with the face
- • 2. Acute progressive psoriasis, and erythroderma tendency
- • 3. current (or within 1 year) pregnancy or lactation
- • 4. current significant anxiety or depression with the Self-rating Anxiety Scale (SAS) \> 50 or the Self-rating Depression Scale (SDS) \> 53, or with other psychiatric disorders
- • 5. With history of primary cardiovascular, respiratory, digestive, urinary, endocrinologic and hematologic diseases, which can't be controlled through ordinary treatments. Those who with malignant diseases, infections, electrolyte imbalance, acid-base disturbance. Patients with clinical test results listed below: abnormal serum calcium level ( Ca2+ \> 2.9 mmol/L or \< 2 mmol/L);AST or ALT 2 times more than normal upper limit; Creatinine and cystatin C more than normal upper limit; Hemoglobin elevates 20g/L more than normal upper limit,or hemoglobin reduction to anemia; Platelet count less than 75.0\*10\^9/L; White blood cell less than 3.0\*10\^9/L; Or any other abnormal laboratory test results, assessed by investigators, that are not suitable for this clinical study
- • 6. Patients with malignant tumors, or when they were enrolled with abnormal tumor markers or with other organ dysfunction
- • 7. allergy to anything else ever before;
- • 8. current registration in other clinical trials or participation within a month;
- • 9. topical treatments (i.e. corticosteroids or retinoic acid or Vitamin D analogs ) within 2 weeks; systemic therapy or phototherapy (ultraviolet radiation B,UVB) and psoralen combined with ultraviolet A (PUVA) within 4 weeks; biological therapy within 12 weeks;
- • 10. medical conditions assessed by investigators, that are not suitable for this clinical study.
About Guangdong Provincial Hospital Of Traditional Chinese Medicine
Guangdong Provincial Hospital of Traditional Chinese Medicine is a leading clinical research institution dedicated to advancing the field of traditional Chinese medicine through rigorous scientific investigation. As a prominent sponsor of clinical trials, the hospital integrates traditional therapeutic practices with modern medical research methodologies to evaluate the efficacy and safety of various treatments. With a commitment to improving patient outcomes and enhancing healthcare practices, the hospital collaborates with multidisciplinary teams to conduct innovative studies that contribute to the global understanding and application of traditional medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Guangzhou, Guangdong, China
Patients applied
Trial Officials
Chuanjian Lu, PhD
Principal Investigator
Guangdong Provincial Hospital of Traditional Chinese Medicine
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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