Assessment of Pro-Resolution Mediator Levels in Periodontitis Stage III and IV Before and After Periodontal Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorCairo University

About this trial

This study aims to assess Pro-Resolution Mediator levels during non-surgical periodontal therapy in individuals with Stage III and IV periodontitis, comparing them to healthy subjects. Periodontitis, a chronic inflammatory condition affecting tooth-supporting tissues, can lead to tooth loss and systemic complications. Understanding the role of pro-resolving lipid mediators in inflammation resolution may offer insights into therapeutic benefits associated with these mediators.

Eligibility criteria

Qualifiers

Adult patients above 18 years old.

Interdental CAL at site of greatest loss ≥5 mm or extending to middle third of the root.

Interdental CAL at site of greatest loss ≥8 mm or extending to apical third of the root.

Probing depth ≥6 mm.

Disqualifiers

1. Pregnancy or lactation. 2. Smoking more than 20 cigarettes. 3. Immuno-inflammatory conditions of the skin and oral mucosa 4. systemic conditions affecting bone turnover and periodontal health status (e.g. endocrine and connective tissue diseases, bisphosphonate antiresorptive therapy, gastrointestinal diseases related to nutrition and mineral metabolism) 5. Periodontal or orthodontic treatment at least 6 months before the start of the study 6. Use of anti-inflammatory and antimicrobial agents within 3 months before sampling

Systemically healthy patients.

Patients with an age range between 16 to 80 years.

Patients have a minimum of 20 teeth.

Trial design

Treatments tested in this trial

  • Professional mechanical plaque control

Treatment groups

22 Participants
are divided into 2 treatment groups

Sponsors and collaborators