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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04446767
Other study ID # P.T REC/017/00482.
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 30, 2020
Est. completion date September 5, 2020

Study information

Verified date February 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Effect of Photobiomodulation With Polarized Light on wound healing and aerobic microflora in Diabetic Foot Ulcer


Description:

Effect of Photobiomodulation With Polarized Light on wound healing and aerobic microflora in Diabetic Foot Ulcer both sexes were included and intervention will be given for two months, wound healing will be assessed by measuring the surface area and the Aerobic microflora will be isolated and controlled on the basis of bio-gram and antibiogram at the beginning and at the end of treatment.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 5, 2020
Est. primary completion date August 30, 2020
Accepts healthy volunteers No
Gender All
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria: 1. The patients with diagnosed diabetic foot ulcer lasting at least 4 weeks ( sized from 0.5 to 2 cm 2. Cooperative and mentally stable patients . Exclusion Criteria: 1. Hepatic patients . 2. Uncontrolled hypertension . 3. Uncontrolled diabetic patients with HbA1c>8.5% . 4. Neurological disorders . 5. Musculoskeletal disorders that interfere with program . 6. Previous history or any sign of DVT .

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
polarized light
bioptron light therapy sessions, about 12 minutes on the foot ulcer 3 sessions per week for about 8 weeks
Other:
Medical Care
Appropriate day-care and principles of local ulcer therapy, washing and bandaging, use of anti exudative, anti-inflammatory and disinfection solutions will be administered to this group, topical antibiotics will be administered based on bio-gram and antibiogram results

Locations

Country Name City State
Egypt Kasr Alaini Cairo

Sponsors (2)

Lead Sponsor Collaborator
Cairo University Princess Nourah Bint Abdulrahman University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Histologic evaluation: Aerobic microflora will be isolated and controlled on the basis of biogram and antibiogram at the beginning and at the end of treatment two months
Primary Wound assessment The wound surface area (ulcer size), lenghth and width will measured using Ruler technique two months
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