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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02131922
Other study ID # MOMT-01A
Secondary ID
Status Recruiting
Phase N/A
First received April 28, 2014
Last updated May 5, 2014
Start date September 2009
Est. completion date September 2014

Study information

Verified date May 2014
Source Jagiellonian University
Contact Marta Czesnikiewicz-Guzik, MD PhD
Phone 66683950
Email maczesni@yahoo.co.uk
Is FDA regulated No
Health authority Poland: Jagiellonian University
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 65 Years
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Intensive Treatment
Intensive Surgical Treatment of Periodontitis
Dental Hygienization Treatment

Drug:
Chlorhexidine (Intensive Treatment)
Chlorhexidine (PerioKIN) (0.2%) implantation in dental pockets

Locations

Country Name City State
Poland J. Dietl Hospital, Department of Internal and Agricultural Medicine, Jagiellonian University Krakow
Poland Jagiellonian University Dental Clinic Krakow

Sponsors (1)

Lead Sponsor Collaborator
Jagiellonian University

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Other Leukocyte Immunophenotype and Cytokine measurement 3 months No
Other Periodontal Health Score - Probing Depth 3 months No
Other Periodontal Health Score - CAL - Clinical Attachment Loss 3 months No
Other The Community Periodontal Index of Treatment Needs Index 3 months No
Other Gingival Index 3 months No
Primary Blood Pressure Change Ambulatory Blood Pressure Monitoring 3 months No
Secondary Flow Mediated Dilatation Vascular Function Measurement 3 months No
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