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NCT ID: NCT03219944 Not yet recruiting - Clinical trials for Thin Gingival Biotype

Clinical Evaluation of Platelet Rich Fibrin Versus Subepithelial Connective Tissue Graft for Soft Tissue Augmentation

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

Soft tissue biotype is a critical factor for success of implant in the esthetic zone . Different soft tissue augmentation techniques have been employed to increase soft tissue thickness such as: autogenous grafts, allografts, xenografts and living cellular construct (LCC). Studies showed that, allografts and xenografts were inferior when compared with autogenous graft . However, few studies were conducted to evaluate the efficacy of soft tissue augmentation with platelet rich fibrin in order to overcome the patient morbidity with SCTG.

NCT ID: NCT03225469 Not yet recruiting - Bowel Preparation Clinical Trials

Improving Effect of Reinforced Family Assistance on the Quality of Bowel Preparation for Colonoscopy

IERFAOBP
Start date: August 15, 2017
Phase: N/A
Study type: Interventional

Enhanced instructions such as re-education by telephone or short message which increase the patient adherence eventually improve the quality of bowel preparation significantly. However, the effect of family assistance which plays an essential role on compliance of patient with treatment on bowel preparation is unknown. The investigators hypothesized that reinforced education giving family members of outpatients will enhance family support to patients for colonoscopy, and consequently improve the quality of bowel preparation. Therefore, the investigators designed protocols to reinforce family member education by verbal (face to face or telephone) and written methods. The aim of this study is to evaluate the effect of reinforced family member education on patient compliance and the quality of bowel preparation for colonoscopy. In addition,the rate of side effects happening, the subjective feelings of bowel preparation, the outcomes of colonoscopy ,and the independent risk factors will be also assessed.

NCT ID: NCT03232502 Not yet recruiting - Depression Clinical Trials

Pharmacogenetics in Primary Care Psychotropics

Start date: August 15, 2017
Phase: Phase 3
Study type: Interventional

Pragmatic trial of pharmacogenetic testing at the time of prescription for a selective serotonin reuptake inhibitor, tricyclic antidepressant or atypical antipsychotic. Does real time intervention improve patient outcomes?

NCT ID: NCT03234855 Not yet recruiting - Physician Feedback Clinical Trials

Laparoscopic Measuring Device Study

LMD-1
Start date: August 15, 2017
Phase: N/A
Study type: Observational

This study is gathering opinions from surgeons on the usability of our laparoscopic measuring device.

NCT ID: NCT03238391 Not yet recruiting - Clinical trials for Contrast-induced Nephropathy

Ischemic Preconditioning for Prevention of Contrast Nephropathy in The Emergency Department

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

The purpose of this study is to demonstrate the effectiveness of ischemic preconditioning in the emergency department to prevent contrast induced nephropathy

NCT ID: NCT03243916 Not yet recruiting - Clinical trials for Hepatocellular Carcinoma

Targeted and Staged Cyber Knife Combined With Interventional Therapy in the Treatment of MHCC

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

Hepatocellular carcinoma is a highly malignant tumor that is progressing rapidly. Hepatic arterial embolization chemotherapy (TACE) is a common method for the treatment of unresectable of hepatocellular carcinoma.But for patients with > 10cm hepatocellular carcinoma, the intervention effect was not satisfied.The cyberknife is a kind of stereotactic radiotherapy which can track the movement of tumor and monitor the position deviation of tumor in real time.This stuy is aimed to observe the efficiency and safety of the combination of TACE and cyberknife in the treatment of massive hepatocellular carcinoma.

NCT ID: NCT03540810 Not yet recruiting - Clinical trials for Primary Antiphospholipid Syndrome

Hydroxychloroquine Versus Placebo: Impact on Thrombotic Relapse in Primary Antiphospholipid Syndrome

PAPIRUS
Start date: August 15, 2018
Phase: Phase 3
Study type: Interventional

Antiphospholipid syndrome (APS) combines thrombotic (venous and/or arterial) and/or obstetrical manifestations, along with biological anomalies related to the presence of antiphospholipid antibodies. Despite actual treatment recommended by international guidelines, the relapse rate in APS is high and survival is 65% at 15 years. Hydroxychloroquine has demonstrated its efficacy and benefits in the treatment of Systemic Lupus Erythematosus, but there is no current consensus concerning the efficacy of this treatment in the secondary prevention of thrombotic events in primary APS, even though several in vitro experimental and animal model data, along with several clinical studies have suggested a beneficial effect of this drug in this indication. Considering the prevalence of primary APS in the general population and of the number of clinical events observed in patients with primary APS and receiving conventional treatment with vitamin K anticoagulants (VKA), the consortium expects a minimum clinically relevant difference of 70%. Considering a prevalence of thrombotic events for the entire studied primary APS population of 10% at 2 years, the consortium expects a 70% decrease in thrombotic events under Hydroxychloroquine treatment administered in addition to VKA treatment in primary APS, i.e. a 3% prevalence in the Hydroxychloroquine group at 2 years. The consortium proposes a drug trial, phase III, national multicentric, comparative, randomized, superiority, double-blind, controlled with 2 compared groups (Hydroxychloroquine versus placebo) study. The enrolment period will be 24 months. The main aim of this trial is to comparatively assess at 24 months the number of new thrombotic events (venous and arterial) in primary antiphospholipid syndrome in patients treated with VKA plus Hydroxychloroquine versus VKA plus placebo, in a multicentre, prospective randomized, double-blind, versus placebo study.

NCT ID: NCT03592875 Not yet recruiting - Nursing Personnel Clinical Trials

Evaluation of Knowledge and Practices in the Systematization of Nursing Care

Start date: August 15, 2018
Phase:
Study type: Observational

Objective to analyse the performance of nurses in the implementation of Nursing Care Systematization - (NCS). This Study is a descriptive research developed from a qualitative approach. The content analysis must be developed through three chronological poles allowing the researcher to construct an analysis structure that corresponds to the needs of the research and the objectives of the proposed research; The chronological poles of content analysis are described as: Phase 1 - Pre-analysis, Phase 2 - Exploration of the material: Phase 3 - Treatment of the results obtained and interpretation. Only a semi-structured interview will be conducted with the research subjects who meet the inclusion criteria of the study, preserving the identity of the individuals and guaranteeing the right to quit the research at any time during the interview.

NCT ID: NCT03599973 Not yet recruiting - Fluid Therapy Clinical Trials

Correlation Between Duration of Fasting and Response to Fluid Replenishment, Evaluated With Repeated Measures of VTI.

Start date: August 15, 2018
Phase: N/A
Study type: Interventional

The investigators will study the correlation between the lenght of the fasting before surgery and the need to replenish with intra-venous fluids in children, evaluated with 3 measures of the aortic Integral Time Velocity with transthoracic echocardiography.

NCT ID: NCT03620799 Not yet recruiting - Clinical trials for Anterior Knee Pain Syndrome

Efffectiveness of a Roller Intervention in Anterior Knee Pain

Start date: August 15, 2018
Phase: N/A
Study type: Interventional

Anterior knee pain is one of the most frequent reasons for consultation within knee conditions in adolescents and young adults. However, despite the high prevalence of this disorder, its pathogenesis and therefore its treatment are not clearly understood. Foam rolling has become a common intervention to enhance joint mobility and muscle recovery after exercise. the aim of this study is analyze the effectiveness of a roller intervention in patients with anterior knee pain.