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Search / Trial NCT06998875

A Retrospective Cohort Study on Primary Cutaneous Amyloidosis

Launched by ARMY MEDICAL UNIVERSITY, CHINA · May 22, 2025

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at a condition called primary cutaneous amyloidosis, which causes skin problems and itching. Researchers want to find out if a combination of two medications, tocilizumab tablets and acitretin capsules, works better than just acitretin alone in relieving itching and improving skin symptoms. They will also check if this combination leads to any unexpected health issues. The study will last 16 weeks, and participants will visit the clinic every four weeks for check-ups.

To be eligible for this study, participants need to be at least 18 years old and have a confirmed diagnosis of primary cutaneous amyloidosis. They should not have any serious underlying health issues or infectious diseases. Participants will take the medications daily and will be monitored closely to see how their symptoms change. It's important to know that they will also be assessed for any side effects during the study. If you or someone you know fits these criteria and is interested, this trial could be an opportunity to help improve treatment options for this skin condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age ≥ 18 years old, without infectious diseases such as "hepatitis B" and "tuberculosis" and major underlying diseases (gender not limited);
  • "Outpatient Diagnosis" includes "primary cutaneous amyloidosis", "macular amyloidosis" or "lichen amyloidosis";
  • Visited the outpatient department for PCA treatment for 4 times or more;
  • The medication record shows "Avastin Capsules" and/or "Tofacitinib Citrate";
  • The medical record fully records baseline characteristics, medication dosage, efficacy assessment and adverse events.
  • Exclusion Criteria:
  • Nodular amyloidosis or combined with other types of amyloidosis (such as systemic amyloidosis);
  • During the study period, other immunosuppressants (such as glucocorticoids, methotrexate) or biologics were used;
  • Incomplete medical records such as demographic data, laboratory parameters, prescription administration and patient prognosis, as well as irregular treatment, etc.

About Army Medical University, China

Army Medical University, located in China, is a leading institution dedicated to advancing military and civilian healthcare through innovative research and education. Renowned for its commitment to medical excellence, the university plays a pivotal role in conducting clinical trials aimed at addressing critical health challenges faced by both military personnel and the general population. With a strong emphasis on translational medicine, Army Medical University integrates cutting-edge scientific research with clinical applications, fostering collaborations that enhance treatment strategies and improve patient outcomes. The institution adheres to rigorous ethical standards and regulatory compliance, ensuring the integrity and reliability of its clinical trial initiatives.

Locations

Chongqing, Chongqing, China

Patients applied

0 patients applied

Trial Officials

Rui Yin, MD

Principal Investigator

Department of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University)

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported