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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04857346
Other study ID # KSU334
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date June 1, 2020
Est. completion date February 1, 2021

Study information

Verified date April 2021
Source King Saud University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

With this design, this study hypothesizes that; (i) ICG-PDT would produce superior clinical, microbiological, and immune-inflammatory outcomes as compared to RSD and (ii) ICG-PDT would produce equal efficacy among different forms of diabetes as produced in non-diabetic subjects and that diabetes mellitus would not produce negative impact on the therapeutic outcomes of ICG-PDT. Therefore, the aim of this randomized controlled clinical trial was to evaluate the efficacy of ICG-mediated aPDT in the treatment of stage III grade C periodontitis among patients with prediabetes, T2DM and non-diabetic subjects.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date February 1, 2021
Est. primary completion date December 12, 2020
Accepts healthy volunteers No
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: 1. aged =30 years 2. clinically diagnosed with mild to moderate periodontitis 3. self-reported type-2 DM for =2 years confirmed by a physician with HbA1c levels =6.5% 4. patients who complied with the treatment protocol. Exclusion Criteria: (i) pregnancy and lactation (ii) who had taken antibiotics in the previous 3 months (iii) who had undergone periodontal therapy or any decontamination treatment in their oral cavity in the previous 6 months (iv) former/current smokers (v) failure to provide a signed informed consent.

Study Design


Intervention

Drug:
Indocyanine green
Single application of PDT will be performed. A diode laser (HELBO®TheraLite - Bredent Medical, Germany) with 670 nm wavelength, power of 150 mW, fluency of 22 J/cm2 and density of 1.1 W/cm2 will be used in this study. Indocyanine-green photosensitizer (Sigm Aldrich, USA) with 0.005% concentration will be used as a photosensitizer which will be applied inside the periodontal pockets in a depth of 3 mm with the help of a blunt needle for 10 s. Laser irradiation will be performed for 60 s using a flexible tip. Laser irradiation will be performed at 2 points each on buccal and lingual with the tip stabilized perpendicular to the gingival tissues.

Locations

Country Name City State
Saudi Arabia College of Applied Medical Sciences, King Saud University Riyadh

Sponsors (1)

Lead Sponsor Collaborator
King Saud University

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Probing depth Probing depth will be measured to the nearest millimeter from the base of the periodontal pocket to the crest of the marginal gingiva. 6 months
Primary Clinical attachment level Clinical attachment level will be measured by adding recession with probing depth 6 months
Secondary Plaque scores Dichotomous scoring to each site of the tooth as '1 - present' and '0 - absent' 6 months
Secondary Bleeding on probing Dichotomous scoring to each site of the tooth as '1 - present' and '0 - absent' 6 months
Secondary Porphyromonas gingivalis Presence or absence of bacteria from the plaque biofilms in the patient 6 months
Secondary Interleukin-6 Proinflammatory cytokine levels that will be quantified in the laboratory. 6 months
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