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Mucositis clinical trials

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NCT ID: NCT04475406 Completed - Peri-Implantitis Clinical Trials

Comparison of Short and Standard Dental Implants

Start date: December 15, 2016
Phase: N/A
Study type: Interventional

Objective: This study aimed to evaluate the total amounts of tumor necrosis factor α (TNF-α), prostaglandin E2 (PGE2), receptor activator of nuclear factor kappa B ligand (RANKL), receptor activator of nuclear factor kappa B (RANK), and osteoprotegerin (OPG) and the abundance of putative oral pathogens Fusobacterium nucleatum, Porphyromonas gingivalis, Treponema denticola, Tannerella forsythia, Prevotella intermedia, and Streptococcus oralis in extra short and standard dental implants functioning in the posterior mandible. Methodology: The implants were divided into two groups according to their lengths: standard (intrabony length ≥8 mm) and extra short (intrabony length ≤ 6 mm). A total of 60 implants were researched in 30 patients. Probing depth (PD), clinical attachment level (CAL), presence of bleeding on probing (BOP), 3-year survival rate (CSR), and bone loss (BL) were measured.

NCT ID: NCT04462341 Terminated - Clinical trials for Peri-implant Mucositis

Efficacy of an Oral Hygiene Implant Protocol

Start date: January 7, 2019
Phase: N/A
Study type: Interventional

This study is designed to evaluate the effectiveness of cleaning around implants that hold a full denture in the mouth. Different oral hygiene protocols will be compared. Areas to measure are gum tissue color and consistency, bleeding and cleanliness. A questionnaire will be provided at the end of the study. This is a proof of concept study.

NCT ID: NCT04440930 Completed - Oral Mucositis Clinical Trials

White Tea for Prevention of Chemotherapy Induced Mucositis

Start date: September 2, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effectiveness of mouthwash with white tea in the prevention of paclitaxel induced oral mucositis in women with breast cancer.

NCT ID: NCT04439877 Completed - Peri-Implantitis Clinical Trials

Exploring the Relationship Among Dental Caries, Nutritional Habits and Peri-implantitis

Start date: February 1, 2018
Phase:
Study type: Observational

Aim: A study was made of the prevalence, co-occurrence and association among caries, nutritional habits and peri-implant disease, with an analysis of the influence of other patient and implant factors upon peri-implant disease. Material and methods: The included subjects underwent a clinical examination and were asked to complete a questionnaire. Demographic data and potential lifestyle/behavioral variables were collected. Clinical and radiographic assessment allowed calculation of the decayed, missing and filled teeth (DMFT) index and peri-implant diagnosis. Uni- and multivariate logistic regression analyses were applied to identify predictors of peri-implant disease.

NCT ID: NCT04421066 Active, not recruiting - Peri-Implantitis Clinical Trials

Histological, Genetic and Epigenetic Analysis of Procedures Related With Dental Implants

Start date: January 29, 2019
Phase:
Study type: Observational [Patient Registry]

In this study genomic, proteomic and histological technologies for the search and characterization of epigenetic modifications and molecular or protein markers, useful in the diagnosis and progression of peri-implant diseases and prevention of implant failure will be used.

NCT ID: NCT04415801 Recruiting - Clinical trials for Peri-implant Mucositis

Effect of Repeated Removal and Re-placement of Abutments Around Dental Implants

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

Repeated removal and re-placement of healing and prosthetic abutments result in frequent injuries to the soft tissues. The purpose was to evaluate the effect of repeated removal and re-placement of laser microgrooved and smooth/machined healing and prosthetic abutments during restorative stages, and 1 year after functional loading, on proinflammatory cytokine levels around dental implants.

NCT ID: NCT04398511 Completed - Oral Mucositis Clinical Trials

L Brevis for Traumatic Oral Lesions in Orthodontic Patients

Start date: January 7, 2019
Phase: Phase 2
Study type: Interventional

Introduction: Traumatic oral lesions are common in the beginning of the orthodontic treatment, and pathogenic oral bacteria might be involved. We tested whether the probiotic Lactobacillus brevis CD2 (L brevis) is benefic in this condition. Methods: In a double-blind clinical trial, 20 patients were randomized to 21 days course of lozenges containing L brevis CD2 (4 billion colony-forming units after breakfast, lunch and dinner) or placebo, starting on the day of installation of the fixed orthodontic appliance. Main outcomes were days without oral lesions and oral pain score [ranging between 0 (no pain) and 10 (maximum)]. Oral health related quality of life was measured by OHIP-14 before and after treatments.

NCT ID: NCT04382079 Recruiting - Oral Mucositis Clinical Trials

Honey Products for Cancer Patients With Oral Mucositis: a Randomized Controlled Trial

Start date: April 8, 2020
Phase: N/A
Study type: Interventional

The investigators plan to conduct a 3-year pioneering care research project for mucositis in cancer patients. These include: (1) an analysis of the incidence and severity of mucositis, severity, treatment methods, and treatment costs; (2) an RCT comparing the effectiveness of honey, Taiwan green propolis, and usual care in mucositis of cancer patients; (3) monitoring of related symptom changes using a smart bracelet device; (4) a measurement of IL-1, IL-6, IL-10, and TNF in saliva and (4) modeling of the trend of mucositis for alertness and search of essential parameters of the complications.

NCT ID: NCT04321850 Terminated - Oral Mucositis Clinical Trials

Impact of the Use of Zinc in the Prevention of Oral Mucositis in Pediatric Patients With Lymphoblastic Acute Leukemia.

Start date: June 10, 2019
Phase: N/A
Study type: Interventional

Oral mucositis (OM) is a secondary complication of chemo/radiotherapy, which causes pain, dysphagia and predisposition to infections, being a frequent reason for hospitalization that may have an impact on the prognosis of cancer patients. Various interventions for the prevention of OM have been studied, including the use of zinc, which is a micronutrient that participates in various cellular functions and in wound repair, while showing a reduction in the incidence and severity of MO, so the purpose of the present study is to evaluate the impact of the use of zinc in the prevention of oropharyngeal mucositis in pediatric patients with acute lymphoblastic leukemia in chemotherapy, comparing it with the use of placebo. Hypothesis: The use of zinc reduces the incidence and severity of OM in pediatric patients with ALL in chemotherapy compared to the control group.

NCT ID: NCT04317183 Recruiting - Clinical trials for Oral Mucositis Due to Chemotherapy

Topical Chamomile in Preventing Chemotherapy-induced Oral Mucositis

Start date: May 15, 2019
Phase: Phase 2
Study type: Interventional

the main aim of this study is to clinically assess the effectiveness of topical chamomile oral gel in the prevention of chemotherapy-induced oral mucositis.