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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04448093
Other study ID # Hemodialysis
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date March 1, 2014
Est. completion date December 20, 2019

Study information

Verified date June 2020
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this work will be to conduct a controlled clinical trial to assess whether the dental treatment of adequacy of the oral environment is capable of generating improvement in the quality of life and self-esteem, comparing the results of patients on hemodialysis who received treatment with others who did not receive treatment .


Description:

After selecting the sample, patients will undergo an oral examination performed by a dental surgeon, in which they will be evaluated for the presence of lesions in the oral mucosa, periodontal conditions through simplified periodontal record - PSR, oral hygiene index, caries and lack of teeth - DMFT, if they need treatment and the situation of the prosthesis, if they use them, the data being recorded in a specific medical record. Subsequently, intervention will be performed in the group that received the treatment (intervention group). The treatment will consist of the adequacy of the oral environment in patients with teeth and evaluation of the mucosa and prostheses for edentulous patients.

The service will take place at the UFVJM Surgery and Periodontics Clinic, on previously scheduled days and times. About 5 to 10 days before treatment, patients answered questionnaires about socioeconomic characterization, self-esteem and quality of life. The therapeutic protocol followed during the service will be the one proposed by Quirynen (1995) [22], in which the debridement of the entire mouth is recommended in a single 45-minute session. After removing the supra and subgingival biofilm, the patient will be instructed to use mouthwashes with 15 ml of 0.12% chlorhexidine gluconate, for one minute, twice a day, thirty minutes after brushing, for seven days. In this phase, emergency extractions, restoration of restorations and cavity closure with glass ionomer cement and resins in the anterior teeth will also be performed, in order to adapt the oral environment in minimal interventions, considering the patient's systemic state.

All patients who have at least 1 tooth, healthy or not, will be considered dentate. Toothless patients will receive guidance on oral hygiene and prostheses, if used, and will also use mouthwash with 0.12% chlorhexidine gluconate for the same period. Group participants who were not submitted to the intervention (control group), received the same initial assessment and answered the same questionnaires, but will not be treated at that time. After 45 days from the end of the dental treatment, everyone will be reassessed, went through oral hygiene instructions again and answered the questionnaires, the questions being directed to the patient's perception in the last 45 days after treatment.


Recruitment information / eligibility

Status Completed
Enrollment 121
Est. completion date December 20, 2019
Est. primary completion date August 29, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 86 Years
Eligibility Inclusion Criteria:

- patients over 18 years

- submitted to hemodialysis

- agreed to participate voluntarily by invitation and sign an informed consent form

Exclusion Criteria:

- severe anemia

- uncontrolled systolic and diastolic blood pressure or greater than 180/110 mmHg

- unstable angina, complex ventricular arrhythmias, severe metabolic disease

- acute myocardial infarction less than a month

- acute conditions, aortic aneurysm, severe aortic stenosis or respiratory impairment

- neurological and / or musculoskeletal that contraindicate treatment

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
dental treatment
Dental treatment of adequacy of oral environment and assessment of quality of life and self-esteem through questionnaires comparing a group that received treatment with another that did not.

Locations

Country Name City State
Brazil Periodontics Clinic, Department of Dentistry Diamantina Minas Gerais

Sponsors (1)

Lead Sponsor Collaborator
Federal University of São Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dental treatment Comparison of quality of life and self-esteem results of patients who underwent dental treatment with others who did not. 6 years
See also
  Status Clinical Trial Phase
Not yet recruiting NCT06394843 - Fluid Currents During Hemodialysis