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NCT ID: NCT02807792 Withdrawn - Clinical trials for Transanal Endoscopic Surgery

Perianal Operating Scope Feasibliity

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

This protocol will test a new prototype of a peri-anal access device, with increased flexible length and a captured operative field, for feasibility in patients immediately prior to their scheduled peri-anal procedure.

NCT ID: NCT02807571 Withdrawn - Surgery Clinical Trials

Office Based Hand Surgery Using WALANT (Wide Awake Local Anesthesia No Tourniquet): Outcomes and Cost Savings Analysis

WALANT
Start date: February 10, 2017
Phase:
Study type: Observational

This study is aimed at determining if office based surgery is an effective way of cutting health care cost while maintaining patient safety and satisfaction.

NCT ID: NCT02807441 Withdrawn - Thrombosis Clinical Trials

Perioperative Bleeding and Aspirin Use in Spine Surgery

ASA
Start date: July 2016
Phase: Phase 3
Study type: Interventional

The investigators would like to further the current understanding of aspirin and its effects on perioperative bleeding by conducting a randomized controlled trial of spinal surgery patients receiving varying doses of aspirin or no aspirin perioperatively. The investigators hypothesize that there will be no significant difference in perioperative blood loss between the different groups.

NCT ID: NCT02806765 Withdrawn - Aging Clinical Trials

Effect of Dietary Supplementation on Dynamic Stability

Start date: September 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether specific nutrient supplementation can improve dynamic stability in older adults.

NCT ID: NCT02805764 Withdrawn - Clinical trials for Obstructive Sleep Apnea

Changes in Upper Airway Anatomy, Quality of Life Measures, and Polysomnographic Parameters Using A Functional Dental Appliance

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

A prospective study measuring changes in upper airway anatomy, quality of life measures, and polysomnographic parameters using a functional dental appliance (Homeoblock)

NCT ID: NCT02803450 Withdrawn - Labor and Delivery Clinical Trials

Epidural Loading: High Volume, Low Concentration

Start date: February 2016
Phase: N/A
Study type: Interventional

This prospective, randomized, single blinded control trial will investigate the effects of epidural loading with a high volume, low concentration local anesthetic solution via the epidural needle versus the epidural catheter.

NCT ID: NCT02803073 Withdrawn - Hypogonadism Clinical Trials

Effect of Testosterone Replacement on Exercise Capacity in Hypogonadal Men After a Recent Myocardial Infarction

Start date: August 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the effects of testosterone replacement in hypogonadal men on exercise tolerance and cardiac rehabilitation after an acute myocardial infarction.

NCT ID: NCT02802436 Withdrawn - Clinical trials for Healing of Extraction Socket

The Impact of a Known Bioactive Agent on the Resolution of Alveolar Socket Preservation

Start date: October 3, 2016
Phase: N/A
Study type: Interventional

The advent of endosseous implant restoration has driven an increasing need for alveolar bone preservation and/or augmentation strategies. Investigations have explored the physical scaffold effects of a wide variety of bone graft materials with each graft material offering a more or less attractive surface for bone deposition. The seeding of these scaffolds with biologically active material seeks to enhance the "osteoconductive" effect by influencing the temporal or sequential steps which result in the desired end product-new bone. Alveolar socket grafts are a common example of these preservation techniques. They are an accepted procedure to maximize the retention of alveolar bone post extraction. They appear to act as a passive scaffold for clot retention and subsequent bone regeneration. The current pilot research project explores addition of a known Bioactive Agent: Platelet Derived Growth Factor (PDGF) to test its impact on healing responses. Histomorphometric assessments will be utilized on microscopic slide material derived from cores trephined as the initial step in the preparation for placement of endosseous dental implants. Outcomes measured will include: Clinical observation of healing response Microscopic measures will be - Measures of residual graft material - New bone formation and new bone contact area with graft - Measures of vascular content - Osteoclast count - Qualitative measures of other marrow components (Cells and relative fiber/ fat content, liner cell characteristics.)

NCT ID: NCT02800889 Withdrawn - Lymphoma Clinical Trials

Dose-Escalation Study of Pixantrone Monotherapy in Pediatric Patients With Relapsed or Refractory Cancer

Start date: October 24, 2016
Phase: Phase 1
Study type: Interventional

This is a phase 1, open-label, dose escalation study to evaluate the safety, pharmacokinetics, and antitumor activity of pixantrone in pediatric patients with relapsed or refractory solid tumors (excluding those with CNS tumors) or lymphoma.

NCT ID: NCT02799758 Withdrawn - Dyslipidemia Clinical Trials

Efficacy & Long-term Safety Comparison Study of NK-104-CR & Livalo® IR With Primary Hyperlipidemia or Mixed Dyslipidemia

Start date: February 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the superior efficacy of NK-104-CR 8 mg daily compared to Livalo® IR 4 mg daily on fasting serum low-density lipoprotein cholesterol (LDL-C) reduction and to evaluate the comparative safety of NK-104-CR 8 mg daily to Livalo® IR 4 mg daily after long-term treatment