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A prospective randomized controlled trial for hibernation therapy for moderate to severe psoriasis

A prospective randomized controlled trial for hibernation therapy for moderate to severe psoriasis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022721
Enrollment
Unknown
Registered
2019-04-23
Start date
2019-04-24
Completion date
Unknown
Last updated
2019-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis

Interventions

Group H:Intravenous injection of scopolamine 0.03mg/kg + propofol 1ug/ml (TCI mode)
Group L:Intravenous injection of scopolamine 0.01mg/kg + propofol 1ug/ml (TCI mode)
Group C:Tropical treatment

Sponsors

Ruijin Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Volunteer to participate in the trial and sign the informed consent form. 2. Commit to comply with the research process and cooperate with the whole process research; 3. 18 to 65 years old, male or female patients; 4. Patients with chronic psoriasis, the duration of disease = 6 months, the skin lesion area = 10% of BSA or PASI score = 12 when enrolled and received first intervention; 5. ASA score I-III.

Exclusion criteria

Exclusion criteria: 1. Patients with other skin diseases that may affect the assessment of severity; 2. The laboratory test results has shown any of the following abnormalities: WBC 15×10^9/L; neutrophil 35kg/m2) or mental disorder cannot cooperate with the assessment of patients; 14. Other circumstances that the investigator believes are not suitable for the trial.

Design outcomes

Primary

MeasureTime frame
PASI score;

Secondary

MeasureTime frame
Serum cytokines;DL-QI scale;

Countries

China

Contacts

Public ContactYu Buwei

Ruijin Hospital, Shanghai JiaoTong University School of Medicine

yubuwei_2013@126.com+86 13801630735

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026