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Treatment for Periodontal Disease in Dialysis Patients (KPU)

Primary Purpose

Periodontal Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Periodontal Scaling and Root Planing
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periodontal Disease focused on measuring Hemodialysis and peritoneal dialysis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Presence of 12 or more teeth
  • Presence of moderate to severe periodontal disease (2 or more teeth with at least 6 mm Clinical Attachment Loss and at least 1 site with Probing Depth > 5 mm)
  • Receiving dialysis for at least 3 months
  • English speaking
  • Ability and willingness to give written informed consent for participation in the study
  • Age 18 to 80 years
  • Twelve or more teeth

Exclusion Criteria:

  • Any severe co-morbid conditions likely to affect life expectancy within 1 year (for example, metastatic cancer)
  • Any condition that would, in the judgement of the clinician, be a contraindication to dental treatment
  • Dementia
  • Pregnancy or lactation
  • Inability to take oral medications
  • Allergy or intolerance to minocycline, tetracyclines or polygycolate polymers
  • Allergy to both penicillin and clindamycin
  • Severe dental caries, pulpal or mucosal disease that would interfere with periodontal therapy
  • Inability or unwillingness to follow the study protocol

Sites / Locations

  • GO Health Center, School of Dentistry, University of North Carolina-Chapel Hill

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Control-delayed periodontal therapy

Intensive Periodontal Therapy

Arm Description

Outcomes

Primary Outcome Measures

Serum Albumin, IL-6, CRP

Secondary Outcome Measures

HbA1c, periodontal probing

Full Information

First Posted
July 9, 2009
Last Updated
May 4, 2012
Sponsor
University of North Carolina, Chapel Hill
Collaborators
OraPharma
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1. Study Identification

Unique Protocol Identification Number
NCT00937976
Brief Title
Treatment for Periodontal Disease in Dialysis Patients
Acronym
KPU
Official Title
Impact of Periodontal Therapy on Metabolic and Inflammatory Markers in Chronic Kidney Disease Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
OraPharma

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective is to test the hypothesis that periodontal intervention in dialysis patients who have both periodontal disease and a historically high burden of cardiovascular disease will result in a reduction of inflammatory markers and improvement markers of nutrition health like albumin. Patients will be randomized to one of two treatment arms: intensive periodontal therapy or control-delayed periodontal therapy. Eligible patients will have 5 study visits over 7 to 12 months.
Detailed Description
The burden of cardiovascular disease (CVD) is well known to those taking care of patients with chronic kidney disease (CKD). Myocardial infarction, sudden death, or stroke, remain leading causes of death and disability, especially for those patients receiving dialysis therapy (Foley 2003). Traditional risk factors (Wilson, D'Agostino et al. 1998) only partially explain the burden of CVD (Longenecker, Coresh et al. 2002). Our research team has been studying the potential role of periodontal disease in explaining the excess burden of CVD in the CKD population. Periodontitis is an inflammatory disease caused by an infection of predominately gram negative organisms (Pihlstrom, Michalowicz et al. 2005) and has been well-studied in other populations as a CVD risk factor (DeStefano, Anda et al. 1993; Mattila, Valtonen et al. 1995; Beck, Garcia et al. 1996; Joshipura, Rimm et al. 1996; Morrison, Ellison et al. 1999; Hujoel, Drangsholt et al. 2000; Wu, Trevisan et al. 2000; Howell, Ridker et al. 2001; Hujoel, Drangsholt et al. 2001; Hung, Willett et al. 2003; Joshipura, Hung et al. 2003; Tuominen, Reunanen et al. 2003; Hung, Joshipura et al. 2004; Pussinen, Alfthan et al. 2004; Pussinen, Nyyssonen et al. 2005; Saremi, Nelson et al. 2005). It has also been demonstrated to accelerate preclinical and clinical atherosclerosis (Loesche, Schork et al. 1998; Arbes, Slade et al. 1999; Genco 1999). In an observational cohort of 168 patients receiving maintenance hemodialysis followed for 18 months, severe and moderate periodontitis was strongly associated with death of cardiovascular causes independent of traditional risk factors (unpublished data). A very high prevalence of periodontal disease in patients with various stages of CKD has been observed. In this population, periodontal disease was associated with a low serum albumin and malnutrition (Kshirsagar, Craig et al. 2007). We present a randomized interventional small exploratory study to assess study feasibility and to determine whether the treatment of periodontal disease in maintenance dialysis patients reduces markers of inflammation and improves markers of nutrition. The existent data support an intervention trial, rather than additional observational studies. There are a multitude of epidemiological studies, including our studies, which confirm an association of periodontal disease and cardiovascular disease (DeStefano, Anda et al. 1993; Mattila, Valtonen et al. 1995; Beck, Garcia et al. 1996; Joshipura, Rimm et al. 1996; Morrison, Ellison et al. 1999; Hujoel, Drangsholt et al. 2000; Wu, Trevisan et al. 2000; Howell, Ridker et al. 2001; Hujoel, Drangsholt et al. 2001; Hung, Willett et al. 2003; Joshipura, Hung et al. 2003; Tuominen, Reunanen et al. 2003; Hung, Joshipura et al. 2004; Pussinen, Alfthan et al. 2004; Pussinen, Nyyssonen et al. 2005; Saremi, Nelson et al. 2005). Thus, the time is right for conducting a hypothesis-driven intervention trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontal Disease
Keywords
Hemodialysis and peritoneal dialysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control-delayed periodontal therapy
Arm Type
Other
Arm Title
Intensive Periodontal Therapy
Arm Type
Other
Intervention Type
Procedure
Intervention Name(s)
Periodontal Scaling and Root Planing
Intervention Description
Participants will take antibiotics prior to dental treatment. Periodontal treatment or a deep cleaning (with local anesthesia or numbing) will be performed to remove plaque and tartar around the teeth and gums. A small amount of antibiotics (minocycline) will be placed around the gums to help fight bacteria and inflammation.
Primary Outcome Measure Information:
Title
Serum Albumin, IL-6, CRP
Time Frame
6 months
Secondary Outcome Measure Information:
Title
HbA1c, periodontal probing
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Presence of 12 or more teeth Presence of moderate to severe periodontal disease (2 or more teeth with at least 6 mm Clinical Attachment Loss and at least 1 site with Probing Depth > 5 mm) Receiving dialysis for at least 3 months English speaking Ability and willingness to give written informed consent for participation in the study Age 18 to 80 years Twelve or more teeth Exclusion Criteria: Any severe co-morbid conditions likely to affect life expectancy within 1 year (for example, metastatic cancer) Any condition that would, in the judgement of the clinician, be a contraindication to dental treatment Dementia Pregnancy or lactation Inability to take oral medications Allergy or intolerance to minocycline, tetracyclines or polygycolate polymers Allergy to both penicillin and clindamycin Severe dental caries, pulpal or mucosal disease that would interfere with periodontal therapy Inability or unwillingness to follow the study protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven Offenbacher, DDS, PhD
Organizational Affiliation
UNC Chapel Hill
Official's Role
Principal Investigator
Facility Information:
Facility Name
GO Health Center, School of Dentistry, University of North Carolina-Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23261122
Citation
Wehmeyer MM, Kshirsagar AV, Barros SP, Beck JD, Moss KL, Preisser JS, Offenbacher S. A randomized controlled trial of intensive periodontal therapy on metabolic and inflammatory markers in patients With ESRD: results of an exploratory study. Am J Kidney Dis. 2013 Mar;61(3):450-8. doi: 10.1053/j.ajkd.2012.10.021. Epub 2012 Dec 20.
Results Reference
derived

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Treatment for Periodontal Disease in Dialysis Patients

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