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Clinical study on the effect of early intervention of phototherapy to improve the healing quality of the thickness skin donor area

Clinical study on the effect of early intervention of phototherapy to improve the healing quality of the thickness skin donor area

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066285
Enrollment
Unknown
Registered
2022-11-30
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

burn

Interventions

Self experiment group:IPL/DPL +Conventional anti scar therapy
Self control group:Conventional anti scar therapy

Sponsors

Shanghai Jiao Tong University Medical School Affiliated Ruijin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 70 Years

Inclusion criteria

Inclusion criteria: The study subjects should meet the following criteria: 1) Signed and dated informed consent form; 2) Commitment to comply with the study procedures and to cooperate with the implementation of the full study; 3) Patients aged 8 to 70 years; 4) Patients without serious cardiovascular and neurological diseases that would affect the observed results or increase the risk of manipulation; 5)Patients with a clear diagnosis of deep II degree and deep II degree or more burns and undergoing STSG surgery; 6) Patients with burns on the torso, buttocks and extremities, with an area between 5% and 30% according to the "rule of nine"; 7)patients with a skin area between 1% and 10% according to the "rule of nine"; 8) The patient's condition is stable

Exclusion criteria

Exclusion criteria: Subjects meeting any of the following criteria will be excluded from this study: 1) Receiving phototherapy other than in this study; 2) The presence of contraindications to the use of lidocaine; 3) Patients with a history of allergy to the test drug; 4) Patients with previous local anesthetic drug intoxication; (5) Combined postoperative complications that would interfere with the observed results; (6) Combined cardiac, pulmonary, hepatic, renal and other important organ insufficiency; (7) Combined with mental illness and serious heart disease, hypertension; (8) Combination of peripheral nervous system diseases or other diseases that can cause abnormal sensation of peripheral nerves; (9) Combination of serious genetic diseases; (10) Combination of severe coagulation disorders; 11)Inadequate clinical information (unclear diagnosis, incomplete medical history, incomplete medication records, etc.); (12) Pregnancy/lactation

Design outcomes

Primary

MeasureTime frame
elasticity;pigment;water content;transepidermal water loss (TEWL);

Countries

China

Contacts

Public ContactBo Yuan

Shanghai Jiao Tong University Medical School Affiliated Ruijin Hospital

hiyuanbo2002@163.com18016060492

Outcome results

None listed

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