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Clinical Trials in China / NCT07682636
Recruiting Observational

Keloid Pathogenesis And Fibroblast Activation Study

NCT07682636 · tracked via the Priya Life Science China tracker
Sponsor
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Phase
Observational
Started
2025-05-10
Last updated
2026-07-06

Condition(s) studied

KeloidsFibroblast

Investigational drug(s) / intervention(s)

Tissue Collection

Tissue Collection: Surgical tissue collection only, no intervention

Study summary

Keloids are benign fibroproliferative skin disorders characterized by excessive fibroblast activation and extracellular matrix deposition. The molecular mechanisms underlying keloid formation remain incompletely understood. This prospective observational study aims to investigate the biological characteristics of keloid tissue by comparing surgically resected keloid specimens with adjacent normal skin obtained from the same patients. Histological and molecular analyses, including histopathology, polymerase chain reaction (PCR), Western blotting, and related laboratory assays, will be performed to identify signaling pathways and key regulatory factors associated with fibroblast activation. The findings may improve the understanding of keloid pathogenesis and identify potential therapeutic targets for future treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Clinically diagnosed with keloid. * Age 18 years or older. * Scheduled to undergo surgical treatment at the study hospital. * Able and willing to provide written informed consent. Exclusion Criteria: * Severe systemic disease. * History of neurologic disease, alcoholism, postherpetic neuralgia, HIV infection, hypothyroidism, diabetes mellitus, or prior cancer chemotherapy. * Other skin diseases within 5 cm of the keloid lesion, such as eczema. * Systemic treatment within 7 days before enrollment or keloid-specific treatment within 6 weeks before enrollment, including intralesional corticosteroid injection, cryotherapy, topical medication, or silicone gel sheeting. * Hormone or immunosuppressive therapy within 3 months before enrollment. * Pregnancy or breastfeeding. * Considered unsuitable for participation by the investigator. * Refusal to participate in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Fourth Affiliated Hospital of Zhejiang University School of Medicine Jinhua China Recruiting

More The Fourth Affiliated Hospital of Zhejiang University School of Medicine trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07682636 on ClinicalTrials.gov ↗ ← All trials in China