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Bone Resorption clinical trials

View clinical trials related to Bone Resorption.

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NCT ID: NCT04279392 Completed - Clinical trials for Bariatric Surgery Candidate

Healthy Body, Healthy Bones After Bariatric Surgery Trial

Start date: September 1, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

One in three adults in the United States suffers from obesity. Bariatric surgery is an increasingly utilized and effective treatment for obesity and obesity-related comorbidities, however, the massive weight loss associated with bariatric surgery adversely affects bone leads to an increased risk of fracture. Bisphosphonate medications, such as zoledronic acid, are used to treat bone loss in patients with osteoporosis, and this study investigates whether this medication can prevent bone loss associated with surgical weight loss procedures.

NCT ID: NCT04261491 Completed - Periodontitis Clinical Trials

Impact of SRP on Bone Resorption and Systemic Inflammatory Markers in Postmenopausal Women With Periodontitis

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study is designed to determine the effect of treating postmenopausal women and using non-surgical techniques on biomarkers of systemic inflammation (IL-6 ) and systemic bone resorption (C-terminal collagen cross-links, CTX).

NCT ID: NCT04259242 Completed - Periodontitis Clinical Trials

SRP, Systemic Inflammation and Serum Bone Resorption Markers Premenopausal Women With Periodontitis and Low BMD

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

To assess the impact of scaling and root planing on systemic inflammation and serum bone resorption markers in pre-menopausal women with periodontitis

NCT ID: NCT04114045 Completed - Inflammation Clinical Trials

Effects of Post-exercise Protein Supplementation in Young Athletes

Start date: December 19, 2016
Phase: N/A
Study type: Interventional

This randomised double blind, placebo-controlled study examined the effects of post-exercise consumption of whey protein (PRO) or carbohydrate (CHO) on performance recovery, muscle damage and inflammatory cytokine responses following a high intensity interval swim (HIIS) in 10-17-year old male and female swimmers.

NCT ID: NCT04054271 Completed - Clinical trials for Implant Tissue Failure

Effects of ABO Blood Types on the Survival and Marginal Bone Resorption of Dental Implants

Start date: December 15, 2017
Phase:
Study type: Observational

This study evaluates implant survival and marginal bone resorption in patients receiving implant treatment with respect to demographic data and AB0 (groups) blood types.

NCT ID: NCT03980847 Completed - Bone Resorption Clinical Trials

Evaluation, the Histomorphometric Study of Nanocrystalline Hydroxyapatite (Nano Bone) Wif Alendronate in the Preservation of the Tooth Socket

Start date: February 23, 2018
Phase: Phase 2
Study type: Interventional

Twenty patients referring to periodontics department of Boroujerd Azad university of dentistry after obtaining consent to participate in teh research project, which TEMPhas more TEMPthan 20 teeth, are over 18 years old and require socket preservation surgery to tooth extraction for teh periodontal problem, caries or Fractures were selected.

NCT ID: NCT03946020 Completed - Bone Resorption Clinical Trials

GBR and Autogenous Bone Chips

Start date: June 1, 2013
Phase: N/A
Study type: Interventional

This study will be an open, prospective, split-mouth, randomised controlled clinical trial. A total of 14 patients searching for oral implant treatment and where a GBR procedure is indicated per implant treatment will be enrolled. All patients have to fulfill all of the inclusion criteria and none of the exclusion criteria. From all patients clinical photos will be taken. Two sites within a patient will be randomly allocated to the 'autologous bone chips and DBBM or 'DBBM particles alone' group. The study will be 1 year follow-up study comprising 9 visits

NCT ID: NCT03899688 Completed - Alveolar Bone Loss Clinical Trials

Tomographic and Histologic Assessment on the Influence of the Use of a Collagen Membrane to Protect the Antrostomy After Maxillary Sinus Floor Augmentation.

Start date: February 20, 2015
Phase: N/A
Study type: Interventional

the aim of the present study was to evaluate the dimensional variation and osseointegration of mini-implants at augmented sinus with the antrostomy left unprotected or protected with a collagen membrane.

NCT ID: NCT03888339 Completed - Dental Implant Clinical Trials

Influence of Abutment Shape on Peri-implant Marginal Bone Loss

Start date: November 5, 2018
Phase: N/A
Study type: Interventional

A study designed as a randomized controlled trial of parallel group design will be conducted at the Dental clinic of the University of Valencia to evaluate the influence of 2.5 mm high abutments with different shapes (commercially available high abutments vs high abutments with modified shape to imitate short abutments) on peri-implant bone loss around bone level implants with platform switching in partially edentulous patients that require a fixed rehabilitation supported by two implants in the posterior mandible or maxilla and in fixed rehabilitation supported by one implant in the anterior mandible or maxilla.

NCT ID: NCT03787875 Completed - Clinical trials for Periodontal Diseases

Impact of Periodontal Treatment on the RANKL/OPG Ratio in Crevicular Fluid

Start date: February 2, 2016
Phase:
Study type: Observational

Objectives: Alveolar resorption is one of the most important events in periodontitis. Osteoclast activity is regulated by the ratio between receptor activator of NF-κB ligand (RANKL) and osteoprotegerin (OPG). The aim of this study was to evaluate changes in the RANKL/OPG ratio in crevicular fluid after periodontal treatment. Material and methods: A total of 15 patients with periodontitis were included in the study group. Samples were collected from an area with active periodontitis and a healthy area. The RANKL and OPG levels were measured before and after periodontal scaling and root planing (SRP) treatment. The study group was compared to the control group, which included 10 patients without periodontitis.