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Interventional Study Targeting Oral Infections in Patients With Chronic Kidney Disease

Not Applicable
Completed
Conditions
Mouth Diseases
Renal Insufficiency, Chronic
Interventions
Other: Intensive oral care & didactic training
Registration Number
NCT02357199
Lead Sponsor
University of Copenhagen
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
93
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intensive oral care & didactic trainingIntensive oral care & didactic trainingProfessional (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 Measures
NameTimeMethod
C-reactive protein, plasmaChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Gingival inflammationChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Gingival inflammation measured by gingivitis index

Secondary Outcome Measures
NameTimeMethod
Periodontal diseaseChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Measurement of attachment level

Saliva composition: SodiumChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Saliva composition: ChlorideChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Saliva composition: PotassiumChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Whole saliva flow rate, stimulatedChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialometry

Saliva composition: Amylase activityChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Whole saliva flow rate, unstimulatedChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialometry

Dental bacterial plaqueChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Measured by plaque index

Saliva composition: Inorganic phosphateChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Saliva composition: Total proteinChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Hematologic status: TransferrinChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Renal function: CarbamideChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Saliva composition: Total calciumChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Saliva composition: AlbuminChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Oral candidiasisChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Smear test

Hematologic status: HemoglobinChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Hematologic status: LeukocytesChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Renal function: BicarbonateChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Renal function: CreatinineChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Renal function: AlbuminChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Oral Health Impact ProfileChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Quality of life questionnaire

Saliva composition: Secretory IgAChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Sialochemistry

Phosphate metabolismChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Hematologic status: ErythrocytesChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Hematologic status: ThrombocytesChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Hematologic status: IronChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Calcium metabolismChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Renal function: PotassiumChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Renal function: SodiumChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Blood sample

Medical Outcomes Study Short VersionChange from baseline examination (before oral care intervention) at 3-months follow-up examination

Quality of life questionnaire

Trial Locations

Locations (1)

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

🇩🇰

Copenhagen, Denmark

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