- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05122117
Impact of Photodynamic Therapy as an Adjunct to Non-surgical Periodontal Treatment on Clinical and Biochemical Parameters Among Patients Having Mild Rheumatoid Arthritis With Periodontitis
Purpose: To evaluate the efficacy of photodynamic therapy (PDT) as an adjunct to non-surgical periodontal therapy on the clinical periodontal and biochemical parameters among patients with rheumatoid arthritis (RA) having periodontitis.
Methods: A total of 50 RA patients with periodontitis were included. The subjects were equally divided into two groups: Group A - scaling and root planning (SRP) + PDT; Group B - SRP only, respectively. Plaque score (PS), bleeding on probing (BOP), pocket depth (PD) and clinical attachment level (CAL) were estimated. The biochemical parameters included the assessment of interleukin 6 (IL-6), tumor necrosis factor-alpha (TNF-α) and rheumatoid factors (RFs). Multiple comparisons were established by employing the Bonferroni's post-hoc test for both clinical and laboratory biomarker data. The Mann-Whitney test was used to compute the p-value for intergroup comparisons. For intra-group comparisons, the p-value was computed with the help of Wilcoxon signed ranks test.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Riyadh, Saudi Arabia, 11451
- King Saud University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients aged ≥25 years
- Satisfying the 2010 ACR/EULAR categorization criteria (with active RA with ≥6 joint involvement and under anti-RA medication ≥3 months)
- Patients having >20 teeth diagnosed with generalized (>30% of sites) chronic periodontitis with PD ≥ 4mm and/or CAL ≥ 4mm and vertical bone loss of at least 4 mm on radiography.
Exclusion Criteria:
- Patients who had underwent periodontal therapy or antimicrobial therapy in the last 6 months
- Any joint replacement
- Pregnancy/lactating mothers
- Patients having other forms of systemic diseases such as diabetes mellitus, hypertension or acquired immunodeficiency syndrome (AIDS)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Methylene blue mediated photodynamic therapy
Methylene blue (MB) with a concentration of 10 mg/mL was delivered inside the periodontal pocket.
MB was injected inside in the selected periodontal pockets 4 - 6 mm with the help of a blunt needle and left for 1 min.
Later, the periodontal pockets were flushed with distilled water for 3 min to remove the excess MB.
The diode laser HELBO® TheraLite - Bredent Medical, Germany) of diameter 200 µm was used to deliver the light to initiate the disinfection process.
Each participant underwent single session of laser exposure.
The laser parameters such as wavelength, spot area, power output and laser energy were set at 660 nm, 0.028 cm2, 60 mW/cm2, and 150 mW, respectively.
The laser was subjected for a period of 30 s in each pocket.
|
Methylene blue (MB) with a concentration of 10 mg/mL was delivered inside the periodontal pocket.
MB was injected inside in the selected periodontal pockets 4 - 6 mm with the help of a blunt needle and left for 1 min.
Later, the periodontal pockets were flushed with distilled water for 3 min to remove the excess MB.
The diode laser HELBO® TheraLite - Bredent Medical, Germany) of diameter 200 µm was used to deliver the light to initiate the disinfection process.
Each participant underwent single session of laser exposure.
The laser parameters such as wavelength, spot area, power output and laser energy were set at 660 nm, 0.028 cm2, 60 mW/cm2, and 150 mW, respectively.
The laser was subjected for a period of 30 s in each pocket.
Other Names:
A single session of full-mouth ultrasonic scaling using a sterilized scaler was rendered to the control group.
Deep pockets were additionally approached and cleaned by using manual 'After Fives' Gracey curette for root planning (Hu Friedy Gracey After Five Vision curette; HuFriedy, Chicago, USA).
This session was followed by a polishing session.
A motivational session was conducted where the patients were educated on the importance of maintaining a good oral hygiene by brushing their teeth twice daily followed by the regular use of dental floss and chlorhexidine mouth wash twice daily, respectively.
Other Names:
|
|
Placebo Comparator: Scaling and root planing
A single session of full-mouth ultrasonic scaling using a sterilized scaler was rendered to the control group.
Deep pockets were additionally approached and cleaned by using manual 'After Fives' Gracey curette for root planning (Hu Friedy Gracey After Five Vision curette; HuFriedy, Chicago, USA).
This session was followed by a polishing session.
A motivational session was conducted where the patients were educated on the importance of maintaining a good oral hygiene by brushing their teeth twice daily followed by the regular use of dental floss and chlorhexidine mouth wash twice daily, respectively.
|
A single session of full-mouth ultrasonic scaling using a sterilized scaler was rendered to the control group.
Deep pockets were additionally approached and cleaned by using manual 'After Fives' Gracey curette for root planning (Hu Friedy Gracey After Five Vision curette; HuFriedy, Chicago, USA).
This session was followed by a polishing session.
A motivational session was conducted where the patients were educated on the importance of maintaining a good oral hygiene by brushing their teeth twice daily followed by the regular use of dental floss and chlorhexidine mouth wash twice daily, respectively.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Probing depth
Time Frame: 12 weeks
|
Measurement of consecutive millimeter markings of the periodontal pocket depth
|
12 weeks
|
|
Clinical attachment level
Time Frame: 12 weeks
|
Measurement of periodontal pocket depth along with recession
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bleeding on probing
Time Frame: 12 weeks
|
Presence or absence of bleeding indicated as '1' or '0', respectively
|
12 weeks
|
|
Plaque index
Time Frame: 12 weeks
|
Presence or absence of plaque indicated as '1' or '0', respectively
|
12 weeks
|
|
Interleukin-6
Time Frame: 12 weeks
|
Assessment from gingival crevicular fluid
|
12 weeks
|
|
Tumor necrosis factor alpha
Time Frame: 12 weeks
|
Assessment from gingival crevicular fluid
|
12 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Immune System Diseases
- Autoimmune Diseases
- Joint Diseases
- Musculoskeletal Diseases
- Rheumatic Diseases
- Connective Tissue Diseases
- Stomatognathic Diseases
- Periodontal Diseases
- Mouth Diseases
- Arthritis
- Arthritis, Rheumatoid
- Periodontitis
- Chronic Periodontitis
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Methylene Blue
Other Study ID Numbers
- 1234786
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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