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Dental Diseases clinical trials

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NCT ID: NCT04492306 Completed - Dental Diseases Clinical Trials

Clinical Evaluation of Dimethyl Sulfoxide Dentin Pre-treatment

Start date: November 17, 2020
Phase: N/A
Study type: Interventional

This study is conducted in order to evaluate the clinical effectiveness of 1% DMSO dentin pre-treatment on the clinical performance of etch and rinse adhesive.

NCT ID: NCT04265768 Recruiting - Wound Heal Clinical Trials

Soft Tissue Changes Around Dental Implants

Geistlich
Start date: June 21, 2021
Phase: N/A
Study type: Interventional

This study aims to characterize the healing pattern following soft tissue augmentation procedure concomitant to implant placement.

NCT ID: NCT04212767 Completed - Dental Diseases Clinical Trials

The Use of PRF in the Management of Soft Tissue Healing

PRF
Start date: April 15, 2017
Phase: N/A
Study type: Interventional

The present study aimed to evaluate the clinical effect of platelet-rich fibrin to improve epithelialization and decrease postoperative pain in post extraction sockets

NCT ID: NCT04191200 Completed - Schizophrenia Clinical Trials

Oral Status of Patients Suffering From SCHIZophrenia Followed at Charles Perrens Hospital

BUCCOSCHIZ
Start date: September 24, 2019
Phase:
Study type: Observational

The aim of the study is to describe the oral health status of patients suffering from schizophrenia and schizoaffective disorders in a psychiatric institute in France.

NCT ID: NCT04153266 Completed - Quality of Life Clinical Trials

Oral Epithelial Dysplasia Informational Needs Questionnaire

ODIN-Q
Start date: October 31, 2018
Phase:
Study type: Observational

Background: Oral epithelial dysplasia (OED) is a condition with an increased risk of oral cancer. Due to the current changes in the factors associated with these diseases (because of human papillomavirus), it is expected that those who have no history of smoking or alcohol, young (<50 years old), and white male would be commonly affected. Those individuals require a higher need for information, preferred a more active role in decision-making, and have a longer lifespan than older individuals. There remain no detailed studies of whether the informational needs delivered to patients with OED met their needs or indeed what information such patient may wish. A few tools are available to evaluate the IN of patients with head and neck disorders. However, the items of these instruments were dedicated to a particular disease (e.g. cancer) and hence are not applicable to be used for OED. Project aims: To evaluate the psychometric properties of the Oral Epithelial Dysplasia Informational Needs Questionnaire (ODIN-Q), developed and revised in the preliminary work for the proposed study, in a cohort of patients with OED. Timescale: 19 months. Clinical significance: This questionnaire can be useful in clinical practice. It could help to meet the patient's information needs and plan educational interventions for those showing unmet needs.

NCT ID: NCT04141215 Recruiting - Bone Resorption Clinical Trials

Allogeneic Bone Paste Versus Allogeneic Bone Powder

Start date: November 15, 2019
Phase: N/A
Study type: Interventional

Autogenous bone graft has been considered the gold standard in Guided Bone Regeneration (GBR) technique used for bone augmentation. However, there are disadvantages associated with autograft use such as limited amount of available bone and increased morbidity for the patient at the sampling site. Several biomaterials have been used as a replacement of the autogenous bone. Viral-inactivated bone allograft powder is an alternative that has proven efficacy and tolerance. This study aims to assess the non-inferiority of viral-inactivated allogeneic bone paste compared to a viral-inactivated cortico-cancellous allogenic bone powder in achieving the ideal bone volume.

NCT ID: NCT04012541 Recruiting - Clinical trials for Acute Myocardial Infarction

Comprehensive Oral Intervention in Patients With AMI

Start date: July 5, 2019
Phase: N/A
Study type: Interventional

The investigators performed a randomized controlled trial with investigator-masked design enrolling subjects with acute myocardial infarction. The purpose of this study is to find a treatment strategy to reduce the risk of recurrence of myocardial infarction through oral hygiene improvement.

NCT ID: NCT04007939 Completed - Clinical trials for Cardiovascular Risk Factor

Personal Lifestyle Engine (PLX) - Personal Lifestyle Medicine Center (PLMC)

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

It has been suggested that the best medicine should include four principles (4P) - Medicine should be personalized, predictive, preventative and participatory. Technology has provided the tools to collect data in ways not previously possible. Individuals can now collect information on their genome (including their genetic predisposition to tolerate medications and to respond to healthy lifestyle programs) that will modify their lifestyle and therapeutic choices. Beyond spot checks of vital signs and weight, individuals can now collect information on body composition, continuous monitoring of heart rate, blood pressure, and even blood sugar. Data on food consumption at a caloric, macronutrient and even micronutrient level can be collected. Standard medical histories and detailed physical examination findings and laboratory biomarkers can be correlated with this data. Collections of individual patient data will need to be managed through computer programs and smart phone applications that provide direct feedback about the influence of lifestyle on health, wellness and biomarkers. To this end, Metagenics is designing and is launching a smart phone application, Personal Lifestyle Engine (PLX), for individual use by patients and their healthcare providers. The statistical analysis of these data is the primary objective of this study.

NCT ID: NCT04005456 Completed - Clinical trials for Cardiovascular Risk Factor

Personalized Lifestyle Intervention for Improving Functional Health Outcomes Using N-of-1 Tent-Umbrella-Bucket Design

LIFE-HOUSE
Start date: September 1, 2018
Phase: N/A
Study type: Interventional

The LIFE-HOUSE research project is designed to evaluate the impact of a personalized lifestyle intervention program on functional capacity as an approach to quantitating health, and its relationship to well understood disease risk determinants. LIFE-HOUSE will utilize an innovative Tent-Umbrella-Bucket design. Participants will gather under the Tent of an all-inclusive 'N of 1' Case Series providing a shelter of Functional Medicine interventions against the storm of chronic disease. Under this Tent are a collection of Umbrellas where participants with similar clinical challenges are evaluated as clinically defined groups with loose guidelines for the planned interventions. Finally, participants standing under these Umbrellas may step into specific Buckets that gather individuals with nearly identical clinical presentations into more formally described prescriptive randomized arms for intervention. Individuals will be offered the opportunity to participate in all Umbrellas and Buckets for which they qualify. They may accept or reject participation in any Umbrella or Bucket and yet remain eligible for participation in the overall Tent.

NCT ID: NCT03851224 Recruiting - Dental Diseases Clinical Trials

Immediate Implant With no Graft , Autogenous Graft or Xenograft.

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Immediate implant placement with no graft , autogenous graft or xenograft with provisionalization.