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NCT ID: NCT03360513 Completed - Clinical trials for Dental Arch Relationship Anomaly

Determining Shapes and Dimensions of Dental Arches for the Use in Lingual Technique.

Start date: August 1, 2016
Phase:
Study type: Observational

This study aims to determine the shape and dimension of dental arches from a lingual perspective, and determine shape and size used for lingual Orthodontics.

NCT ID: NCT03359551 Completed - Choroideremia Clinical Trials

Natural History of the Progression of Choroideremia Study

NIGHT
Start date: June 30, 2015
Phase:
Study type: Observational

The objective of this natural history study is to gain a better understanding of the progression of choroideremia (CHM) and add to the knowledge base for this rare disease.

NCT ID: NCT03359213 Completed - Clinical trials for Mucopolysaccharidosis II

A Study of JR-141 in Patients With Mucopolysaccharidosis II

Start date: July 26, 2018
Phase: Phase 2
Study type: Interventional

A Phase II open-label, randomized, parallel group, 2 sites (Brazil), designed to evaluate the safety and efficacy of 3 doses of study drug for the treatment of the MPS II.

NCT ID: NCT03359200 Completed - Clinical trials for Intraocular Pressure

Analysis of the Microbiota in Goldmann Applanation Tonometers at a Reference Service in Goiânia

Start date: September 1, 2017
Phase: N/A
Study type: Observational

This study aims to evaluate the microbiota of goldmann tonometers and its possible change over the visits

NCT ID: NCT03359070 Completed - Tinea Cruris Clinical Trials

Clinical Trial Comparing Dapaconazole Versus Miconazole in Patients With Tinea Cruris

Start date: January 29, 2014
Phase: Phase 2
Study type: Interventional

This trial aims to evaluate the efficacy of dapaconazole tosylate 2% cream in the treatment of Tinea cruris compared to the active control miconazole nitrate 2% cream in patients with a single lesion.

NCT ID: NCT03359057 Completed - Contraception Clinical Trials

Trial Evaluating Folic Acid Supplementation by Concomitant Administration of Ethinyl Estradiol + Levonorgestrel

Start date: February 26, 2013
Phase: Phase 3
Study type: Interventional

This trial evaluated folic acid supplementation after oral administration of the ethinyl estradiol + levonorgestrel + folic acid (0.02 mg + 0.10 mg + 0.4 mg) coated tablet (Level-Fol® Biolab Sanus Farmacêutica, São Paulo, Brazil) in healthy female volunteers, based on statistical comparisons of folate levels in erythrocytes. Its safety and tolerability was also evaluated.

NCT ID: NCT03358875 Completed - Clinical trials for Non-small Cell Lung Cancer

Comparison of Efficacy and Safety of Anti-PD-1 Antibody BGB-A317 Versus Docetaxel as Treatment in the Second- or Third-line Setting in Participants With NSCLC

Start date: November 30, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to show that BGB-A317 will improve overall survival in participants with Stage IIIB or IV non-small cell lung cancer when compared to docetaxel in second or third-line treatment setting.

NCT ID: NCT03357068 Completed - Bone Resorption Clinical Trials

Effect of Citric Acid Demineralization on Autogenous Bone Blocks Consolidation in Humans

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

This study evaluates the effect of citric acid demineralization in autogenous bone blocks consolidation. Half of participants will receive citric acid treatment at the bone block and recipient site. Other half will receive no demineralization treatment.

NCT ID: NCT03356886 Completed - Low Back Pain Clinical Trials

Additional Effect of Pain Neuroscience Education to Spinal Manipulative Therapy in Chronic Low Back Pain

Start date: November 30, 2017
Phase: N/A
Study type: Interventional

Objectives: The primary objective will be to investigate the additional effect (immediate and after one-month follow up) of pain neuroscience education (PNE) to Spinal Manipulative Therapy (SMT) on primary outcomes of pain intensity and disability in patients with chronic nonspecific low back pain (CLBP).

NCT ID: NCT03356431 Completed - Clinical trials for Osteoarthritis, Knee

Comparison Between Supervised Group Exercise and Home Exercise Program for Knee Osteoarthritis

Start date: April 18, 2017
Phase: N/A
Study type: Interventional

Physical exercise is a widely recommended treatment modality for osteoarthritis, which can be performed through a supervised group exercise or a home exercise program. However, up to now only little research has been conducted on the home exercise program in Brazil. The objective of this study is to compare the efficacy between supervised group exercise and home exercise program in people with knee osteoarthritis. Methods: The study population consists of 46 men and woman with knee osteoarthritis aged between 40 and 65. The patients should be clinically diagnosed with knee osteoarthritis and classified in Kelgreen-Laurence grades I, II and III. Primary outcomes are the Westerm Ontário and McMaster Universities (WOMAC), Lower Extremity Functional Scale (LEFS), Pain Catastrophizing Scale (PCS), Tampa Scale for Kinesiophobia, 40-meter walk test, isometric strength of hip (abduction and adduction) and knee (flexion and extension) and postural control. The patients are randomized into 2 groups, with one group receiving 12 sessions of supervised group exercise and the other group following an exercise program at home. The program lasts 6 weeks with both groups receiving the same exercise protocol consisting of stretching, isometric and isotonic exercises for major muscle groups in both lower extremities. The Mann-Whitney U test is used to examine the Anthropometric variables. The ANOVA is used to compare outcomes before and after treatment. A value of p< 0.05 is considered to be statistically signifcant.