Evaluation of the Effect of light emitting diodes therapy (LEDT) to Reduce the Recovery Period of Rhinoplasty

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20111121008146N36

Enrollment

Registered

2021-11-24

Start date

2021-11-22

Completion date

Unknown

Last updated

2021-11-29

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

Conditions

Rhinoplasty.

Interventions

Intervention 1: Intervention group: 660 nm low power diode laser device treatment procedure with a dose of 4 joules per square centimeter, continuous 10 sessions every other day for 20 days. Intervent

Eligibility

Sex/Gender

All

Age

30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age range between 30 and 70 years Complete consent to participate in the study

Exclusion criteria

Exclusion criteria: Diabetes Pregnant and lactating Sensitivity to light Under 30 and over 70, History of seizures and hypertension in the disease (secondary hypertension)

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: VAS.;Ecchymosis. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: Based on the review of daily photos, we divide them into the following categories: no ecchymosis, mild ecchymosis, moderate and severe.;Swelling. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: Based on the review of daily photos, we divide them into the following categories: no swelling, mild, moderate and severe swelling.;Wound healing. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: Based on the comparison of incision wounds.	—

Measure

Time frame

Pain. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: VAS.;Ecchymosis. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: Based on the review of daily photos, we divide them into the following categories: no ecchymosis, mild ecchymosis, moderate and severe.;Swelling. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: Based on the review of daily photos, we divide them into the following categories: no swelling, mild, moderate and severe swelling.;Wound healing. Timepoint: After surgery, Three days later, one week later, ten days later and 15 days later. Method of measurement: Based on the comparison of incision wounds.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Barati

Shahid Beheshti University of Medical Sciences

laser.cntr@yahoo.com+98 21 2271 8021

Outcome results

None listed

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