Overview
Study of the Effects of Intensive Treatment of Periodontitis on Blood Pressure Control
Status:
Unknown status
Unknown status
Trial end date:
2014-09-01
2014-09-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Hypertensive patients with chronic periodontitis will be randomized to either intensive treatment or supragingival hygienic treatment and the effects on blood pressure will be identified.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Jagiellonian UniversityTreatments:
Chlorhexidine
Chlorhexidine gluconate
Criteria
Inclusion Criteria:- Periodontitis with three or more periodontal pockets with a probing depth (PD) > 5mm
- Bleeding of these periodontal pockets on probing
- Have at least 20 natural teeth
- Provide informed consent and willingness to cooperate with the study protocol
- Age >25 years old
- Absence of other significant oral infections.
- Primary Hypertension on stable treatment
Exclusion Criteria:
- Clinical symptoms of acute inflammatory disorders incl flu, rhinitis, sinusitis etc.
within past 3 weeks
- Hospitalization for any reason within the past 3 months; Life expectancy of < 3 years;
- Allergic disorders; History of chronic infectious disease, Chronic Obstructive
Pulmonary Disease (COPD), tuberculosis; chronic hepatitis B or C infection;
interstitial pneumonitis, bronchiectasis; known chronic pericardial effusion, pleural
effusion, or ascites; liver disease;
- Other known chronic inflammatory or autoimmune condition such as lupus or rheumatoid
arthritis, ulcerative colitis or Crohn's disease
- Secondary hypertension (known plasma renin screening, abdominal ultrasound with
doppler and other investigations)
- Non-basal cell malignancy or treated myelo or lymphoproliferative disease within the
past 5 years;
- Known HIV positive; Immunizations within past 3 months
- Individual requires chronic oxygen support or mechanical ventilation other than
nocturnal respiratory support for sleep apnea.
- Primary pulmonary hypertension.
- Use of systemic or local steroids or immunosuppressive agents within 6 months of the
inclusion.
- Individual is pregnant or nursing
- History of alcohol abuse or unwillingness to limit alcohol consumption to less than 4
drinks per week