Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
100 participants
OBSERVATIONAL
2012-01-01
2024-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Retrospective Analysis of Spray Skin Treats for Severe Burns
NCT06170424
Research on the Key Technology of Burn Wound Treatment
NCT03279549
Negative Pressure Wound Therapy for Skin Grafts
NCT02374528
Laser Therapy for Treating Hypertrophic Burn Scars in Children
NCT01653691
SSD vs Collagenase in Pediatric Burn Patients
NCT00787592
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experiment gourp
Autologous skin cell suspension combined with autologous skin graft was used to treat burn wound
spray skin
autologous skin cell suspension combined with skin graft
Control group
Autologous skin graft was used to treat burn wound
skin graft
skin graft
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
spray skin
autologous skin cell suspension combined with skin graft
skin graft
skin graft
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Children
Exclusion Criteria
* Congenital immune disease
* Severe cardiopulmonary failure，etc
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
First Affiliated Hospital, Sun Yat-Sen University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hu Zhicheng
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jiayuan Zhu
Role: PRINCIPAL_INVESTIGATOR
First Affiliated Hospital, Sun Yat-Sen University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Burn Surgery, The First Affiliated Hospital of Sun Yat-sen University
Guangzhou, Guangdong, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SYSU-FAH-20231208
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.