search
Back to results

Interventional Study Targeting Oral Infections in Patients With Chronic Kidney Disease

Primary Purpose

Mouth Diseases, Renal Insufficiency, Chronic

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Intensive oral care & didactic training
Sponsored by
University of Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Mouth Diseases focused on measuring Mouth Diseases, Renal Insufficiency, Chronic, Intervention Studies

Eligibility Criteria

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

Inclusion Criteria:

  • Patients on a kidney transplant waiting list or patients who have had a kidney transplant (1-1½ year previously)
  • Dentate patients (>10 teeth)
  • Age >18 years
  • Danish language

Exclusion Criteria:

  • Patients not capable of following the research protocol
  • Legally unavailable
  • Need of antibiotic prophylaxis with dental treatment
  • Heart valve surgery

Sites / Locations

  • Department of Odontology, Faculty of Health Sciences, University of Copenhagen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intensive oral care & didactic training

Standard oral care

Arm Description

Professional (dental hygienist) intensive oral care intervention and individual patient training/didactic instruction to promote patient compliance and patient capability of oral preventive measures in a long-term perspective.

Standard oral care protocol consisting of referral by staff in the Department of Nephrology to general dental practitioner followed by patient self-administration of tooth brushing, fluoride toothpaste and oral lubricants.

Outcomes

Primary Outcome Measures

Gingival inflammation
Gingival inflammation measured by gingivitis index
C-reactive protein, plasma
Blood sample

Secondary Outcome Measures

Dental bacterial plaque
Measured by plaque index
Periodontal disease
Measurement of attachment level
Whole saliva flow rate, unstimulated
Sialometry
Whole saliva flow rate, stimulated
Sialometry
Saliva composition: Sodium
Sialochemistry
Saliva composition: Chloride
Sialochemistry
Saliva composition: Potassium
Sialochemistry
Saliva composition: Total calcium
Sialochemistry
Saliva composition: Inorganic phosphate
Sialochemistry
Saliva composition: Total protein
Sialochemistry
Saliva composition: Albumin
Sialochemistry
Saliva composition: Amylase activity
Sialochemistry
Saliva composition: Secretory IgA
Sialochemistry
Oral candidiasis
Smear test
Hematologic status: Erythrocytes
Blood sample
Hematologic status: Hemoglobin
Blood sample
Hematologic status: Leukocytes
Blood sample
Hematologic status: Thrombocytes
Blood sample
Hematologic status: Transferrin
Blood sample
Hematologic status: Iron
Blood sample
Calcium metabolism
Blood sample
Phosphate metabolism
Blood sample
Renal function: Carbamide
Blood sample
Renal function: Bicarbonate
Blood sample
Renal function: Creatinine
Blood sample
Renal function: Albumin
Blood sample
Renal function: Potassium
Blood sample
Renal function: Sodium
Blood sample
Oral Health Impact Profile
Quality of life questionnaire
Medical Outcomes Study Short Version
Quality of life questionnaire

Full Information

First Posted
January 28, 2015
Last Updated
August 28, 2015
Sponsor
University of Copenhagen
Collaborators
Rigshospitalet, Denmark, Danish Council for Independent Research - Medical Sciences, The Danish Dental Association
search

1. Study Identification

Unique Protocol Identification Number
NCT02357199
Brief Title
Interventional Study Targeting Oral Infections in Patients With Chronic Kidney Disease
Official Title
Interventional Study Targeting Oral Infections in Patients With Chronic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Copenhagen
Collaborators
Rigshospitalet, Denmark, Danish Council for Independent Research - Medical Sciences, The Danish Dental Association

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study aims to investigate the prevalence of oral infection in chronic renal disease patients and to examine whether a focused oral hygiene intervention can reduce oral infection leading to reduced systemic inflammatory parameters in chronic renal disease patients in hemodialysis, chronic renal disease patients waiting for kidney transplantation, and chronic renal disease patients who has been transplanted 1-1½ year previously. The results will be compared to a gender- and age-matched healthy control group.
Detailed Description
Aim: The aim is to examine if a focused oral care procedure to reduce oral infection will be mirrored in reduction of systemic inflammatory parameters in chronic renal disease patients. Specific research questions: Can oral infection and systemic inflammatory parameters in chronic renal disease patients be reduced by 1 month of professional oral care and individual prophylactic instruction and can a potential reduction of inflammation be continuously achieved at a 3 months follow-up. Study design: Randomized, double-blinded (investigator, outcomes assessor), controlled study. For Eligibility Criteria and Outcome Measures, please see elsewhere in the ClinicalTrials.gov Protocol Registration System. Participants: A: Hemodialysis patients, inclusion n=34, B: Hemodialysis patients on a kidney transplant waiting list, inclusion n=34, C: Patients who have had a kidney transplant (1-1½ years after transplantation), inclusion n=34. D: Gender- and age-matched healthy control group. Number of included patients is estimated from a hypothesis-generating pilot study, a statistical power analysis and the estimated loss to follow-up based on experience from previous research projects in the Nephrology Department. Intervention and control: The intervention consists of professional oral care (addressing periodontal and oral mucosal infections, salivary gland dysfunction and caries prevention) and a didactic approach to individual instruction in oral hygiene/prophylactic measures performed by a dental hygienist at three visits: baseline, 2 weeks after baseline and 1 month after baseline. The research data will be registered by a blinded investigator before the first visit at the dental hygienist and after 3 months. The control group will follow best-clinical-practice procedures currently implemented in the hospital.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mouth Diseases, Renal Insufficiency, Chronic
Keywords
Mouth Diseases, Renal Insufficiency, Chronic, Intervention Studies

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
93 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intensive oral care & didactic training
Arm Type
Experimental
Arm Description
Professional (dental hygienist) intensive oral care intervention and individual patient training/didactic instruction to promote patient compliance and patient capability of oral preventive measures in a long-term perspective.
Arm Title
Standard oral care
Arm Type
No Intervention
Arm Description
Standard oral care protocol consisting of referral by staff in the Department of Nephrology to general dental practitioner followed by patient self-administration of tooth brushing, fluoride toothpaste and oral lubricants.
Intervention Type
Other
Intervention Name(s)
Intensive oral care & didactic training
Intervention Description
Professional (dental hygienist) intensive oral care intervention and individual patient training/didactic instruction to promote patient compliance and patient capability of oral preventive measures in a long-term perspective.
Primary Outcome Measure Information:
Title
Gingival inflammation
Description
Gingival inflammation measured by gingivitis index
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
C-reactive protein, plasma
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Secondary Outcome Measure Information:
Title
Dental bacterial plaque
Description
Measured by plaque index
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Periodontal disease
Description
Measurement of attachment level
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Whole saliva flow rate, unstimulated
Description
Sialometry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Whole saliva flow rate, stimulated
Description
Sialometry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Sodium
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Chloride
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Potassium
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Total calcium
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Inorganic phosphate
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Total protein
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Albumin
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Amylase activity
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Saliva composition: Secretory IgA
Description
Sialochemistry
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Oral candidiasis
Description
Smear test
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Hematologic status: Erythrocytes
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Hematologic status: Hemoglobin
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Hematologic status: Leukocytes
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Hematologic status: Thrombocytes
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Hematologic status: Transferrin
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Hematologic status: Iron
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Calcium metabolism
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Phosphate metabolism
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Renal function: Carbamide
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Renal function: Bicarbonate
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Renal function: Creatinine
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Renal function: Albumin
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Renal function: Potassium
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Renal function: Sodium
Description
Blood sample
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Oral Health Impact Profile
Description
Quality of life questionnaire
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Title
Medical Outcomes Study Short Version
Description
Quality of life questionnaire
Time Frame
Change from baseline examination (before oral care intervention) at 3-months follow-up examination
Other Pre-specified Outcome Measures:
Title
Dental caries
Description
Clinical registration of dental caries
Time Frame
Baseline examination (before oral care intervention), 3-months follow-up examination

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients on a kidney transplant waiting list or patients who have had a kidney transplant (1-1½ year previously) Dentate patients (>10 teeth) Age >18 years Danish language Exclusion Criteria: Patients not capable of following the research protocol Legally unavailable Need of antibiotic prophylaxis with dental treatment Heart valve surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siri B Jensen, DDS, PhD
Organizational Affiliation
University of Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Odontology, Faculty of Health Sciences, University of Copenhagen
City
Copenhagen
ZIP/Postal Code
DK-2200
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
18701615
Citation
Kato S, Chmielewski M, Honda H, Pecoits-Filho R, Matsuo S, Yuzawa Y, Tranaeus A, Stenvinkel P, Lindholm B. Aspects of immune dysfunction in end-stage renal disease. Clin J Am Soc Nephrol. 2008 Sep;3(5):1526-33. doi: 10.2215/CJN.00950208. Epub 2008 Aug 13.
Results Reference
background
PubMed Identifier
9438096
Citation
McIntyre C, Harper I, Macdougall IC, Raine AE, Williams A, Baker LR. Serum C-reactive protein as a marker for infection and inflammation in regular dialysis patients. Clin Nephrol. 1997 Dec;48(6):371-4.
Results Reference
background
Citation
Thorman R. Oral health in patients with chronic kidney disease. Stockholm, Sweden: Karolinska Institutet; 2009
Results Reference
background

Learn more about this trial

Interventional Study Targeting Oral Infections in Patients With Chronic Kidney Disease

We'll reach out to this number within 24 hrs