explorative study for the efficacy of low level laser therapy for the prevention of radiodermatitis

Explorative study for the efficacy of 633nm and 830nm wavelength Low level laser therapy for the PRevention of RAdiodermatitis :comparative study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004950

Enrollment

Registered

2020-04-21

Start date

2018-12-04

Completion date

Unknown

Last updated

2020-05-18

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

Conditions

None listed

Interventions

Medical Device : This study is conducted for patients who are planning to undergo radiotherapy after breast cancer surgery. Surgery is divided into two groups, total mastectomy and breast conservative

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: a)10 patients who have undergone breast conservative surgery and 10 patients who have undergone total mastectomy b) Adult aged from 19 to 65 c) ECOG performance status 0-1 d)A person who voluntarily signs a written agreement in informed consent document and who can be followed up during the study period.

Exclusion criteria

Exclusion criteria: a) Patients who are of become pregnant b) Patients who have photosensitivity history c) Patients who are unable to comply with the provisions of the clinical trial. d) Inappropriate patients for this tiral judged by clinicians or investigators

Design outcomes

Primary

Measure	Time frame
severity of radiodermatitis, the difference of moisture, sebum, TEWL, erythema and pigment index between irradiated breast and the opposite breast	—

Secondary

Measure	Time frame
adverse event, inconvenience	—

Countries

Korea, Republic of

Contacts

Public ContactJI HYE PARK

Samsung Medical Center

Outcome results