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NCT ID: NCT04193397 Completed - Bariatric Surgery Clinical Trials

Effects of Physical Training on Health Markers of Post-bariatric Patients

Obesity
Start date: December 1, 2022
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to study the effects of resistance training program on physical-functional fitness, muscle mass and strength, endothelial function, blood pressure, biochemical markers of cardiovascular risk and bone metabolism, density and microstructure and quality of life of post-bariatric patients (Study 1). To compare the bone and muscle changes in post-bariatric patients by Roux-en-Y Gastric Bypass Surgery with non-bariatric controls, as well as to correlate these health indicators with surgery time and weight loss (Study 2).

NCT ID: NCT04193384 Completed - Obesity Clinical Trials

Predictive Factors of Regain in Bariatric Patients Without Outpatients Care Regular.

Obesity
Start date: November 1, 2018
Phase:
Study type: Observational

The bariatric surgery is recommended for treatment of patients with severe obesity, resulting in greater weight loss and improvement of cardiovascular and metabolic comorbidities. However, weight regain is observed in patients after surgery, leading to health adverse outcomes. The purpose of this study is to identify the rate of weight regain and predictive factors of regain in bariatric patients without outpatients care regular.

NCT ID: NCT04192994 Completed - Endophthalmitis Clinical Trials

Evaluation do Early Pars Plana Vitrectomy in Acute Endophthalmitis

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

Our study will evaluate the efficacy of early PPV in acute endophthalmitis and attempt to prove its greater effectiveness for combating infection when compared to eyes that received only intravitreal antibiotic therapy

NCT ID: NCT04192565 Completed - Clinical trials for Colorectal Neoplasms

A Prospective Investigation of the ColubrisMX ELS System

Start date: September 9, 2020
Phase: N/A
Study type: Interventional

This study is a prospective, single-arm, open-label, multi-center, feasibility study to evaluate the safety and efficacy of ColubrisMX ELS System in patients undergoing transanal endoluminal procedures, specifically colorectal Endoscopic Submucosal Dissection.

NCT ID: NCT04187222 Completed - Mucositis Oral Clinical Trials

Effect of Probiotic Use Bifidobacterium Animalis Subsp. Lactis in Peri-implant Mucositis

Mucosite prob
Start date: July 1, 2018
Phase: Phase 3
Study type: Interventional

Peri-implant disease is an inflammatory process of bacterial etiology that can affect the tissues around the implants and can be classified as peri-implant mucositis or peri-implantitis. The confirmation of the action of probiotics against microorganisms that cause peri-implant diseases can represent a great advance in the treatment of these diseases that affect a large part of the population, and may even reduce or prevent the use of antibiotics, reducing the risk of implant loss and, consequently, greater damage to the oral and systemic health of individuals. The purpose of this study was to evaluate the action of probiotics on the peri-implant health of total edentulous patients using Branemark protocol prosthetic rehabilitations. For this, 38 patients were selected, without systemic alterations and non-smokers. Clinical monitoring was performed at baseline (pre-intervention period) as well as at 12 and 24 weeks after study initiation. The following parameters were evaluated: modified gingival index (MGI), modified plaque index (MPI), probing depth (PD) and probing bleeding (PB). Data were subjected to statistical analysis at a significance level of 5%. There was an increase in sites with IGM 0 in the test group at 12 and 24 weeks. The test group presented more sites with IGM 0 than the control. IPM 0 sites increased in the control group at 12 and 24 weeks in the control group. PD decreases in a test and control group. Finally, the test group had lower PB rates. Thus, the probiotic used demonstrated ability to contribute to the improvement of peri-implant health of the patients analyzed.

NCT ID: NCT04187001 Completed - Neck Pain Clinical Trials

Home Exercises Protocol for Neck Pain

Start date: May 13, 2018
Phase:
Study type: Observational [Patient Registry]

Delphi study about home exercise protocol development for neck pain.

NCT ID: NCT04186780 Completed - Dyslipidemias Clinical Trials

Effects of Lentinula Edodes Bars on Dyslipidemia and Oxidative Stress in Cholesterol Individuals: Randomized Study

Start date: September 26, 2018
Phase: N/A
Study type: Interventional

The daily change in population routine has stimulated the development of health beneficial value added products. Lentinula edodes (Shiitake) is a mushroom with high protein concentration, low lipid content, rich in fiber, minerals, vitamins, antioxidant compounds, β-glucans and chitosan. This is clinical study phase II, randomized, double-blind for analyze in the effect of eating Shiitake bars on cholesterolemia and oxidative stress levels in individuals with borderline cholesterol. Individuals with at least one of the following biochemical markers (total cholesterol, LDL or triglycerides) at the borderline level were recruited through online questionnaire. Individuals (n = 68) were randomly allocated to two groups (Group I - Shiitake free bar (n = 32); Group II - Shiitake bar (n = 36). Each individual underwent blood collection at 0, 33 and 66 days, and received an unidentified opaque bag containing the bars.Biochemical analyzes (triglycerides, total cholesterol, LDL, HDL and glucose) and oxidative stress markers (Catalase, GSH and TBARS) were performed on samples of individuals.

NCT ID: NCT04186767 Completed - Obesity Clinical Trials

Weight Loss Impact on Male Fertility

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

This is a prospective non-randomized unicentric clinical trial, characterized by the inclusion of obese (BMI> 35) male with subfertility (sperm count showing low sperm counts and / or motility and / or morphology and / or DNA fragmentation). Patients selected at the endocrinology obesity HC-FMUSP outpatient will be submitted to very low calorie diet (VLCK) for 6 months, being reassessed clinically and laboratorially monthly.

NCT ID: NCT04182542 Completed - Adiposity Clinical Trials

Effects of Capacitive Radiofrequency at the Dermis and Adipose Tissue

Start date: December 2, 2019
Phase: N/A
Study type: Interventional

Noninvasive fat reduction is a rapidly expanding field of cosmetic rejuvenation, as many patients are unwilling to suffer the downtime and healing associated with traditional invasive liposuction. The radiofrequency (RF) device has been shown to be safe and effective for non-invasive fat reduction, as well as cutaneous enhancement and improvement of skin flaccidity (BOISNIC, et al., 2014).

NCT ID: NCT04182191 Completed - Pain Clinical Trials

Influence of CYP2C9 Genotype on Clinical Efficacy of Tenoxicam

Start date: March 1, 2018
Phase: Phase 4
Study type: Interventional

The goal of this study is to evaluate the different gene haplotypes for the clinical efficacy of tenoxicam after third lower molar surgery for pain, edema and trismus, adverse reactions, need of rescue medication, patient satisfaction regarding the drug and the pharmacokinetics of the drug between the different gene haplotypes for CYP2C9 that are found in this population