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NCT ID: NCT01962883 Completed - Clinical trials for Post Concussion Syndrome

Effects of Osteopathic Treatment on Vestibular Disturbed Active Post Concussed Individual

PCS
Start date: August 2013
Phase: N/A
Study type: Interventional

The proposed study is a randomized clinical trial with the purpose of determining the efficacy of osteopathic treatment on vestibular symptoms of the post concussed vestibular disturbed athlete as determined by the Dizziness Handicap Inventory (DHI) and the Balance Error Scoring System (BESS). Of secondary interest, this study will evaluate the osteopathic assessment findings of this population and side effects, positive and negative, associated with the osteopathic treatment provided. Primary Hypothesis 1. Osteopathic treatment will have no effect on the symptoms of dizziness of the vestibular disturbed post concussed athlete using the Dizziness Handicap Inventory 2. Osteopathic treatment will have no effect on the balance recovery of the vestibular disturbed post concussed athlete using Balance Error Scoring System (BESS) Secondary Hypothesis 3. To determine the side effects of osteopathic treatment of the vestibular disturbed post concussed athlete

NCT ID: NCT01962831 Completed - Obesity Clinical Trials

Randomized Controlled Trial: Induction of Labour of Obese Women With Dinoprostone or Single Balloon Catheter

Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of single balloon foley catheters to dinoprostone for the induction of labour of obese women. The investigators suspect that women assigned to the foley group will have a shorter induction to delivery time than women in the dinoprostone group.

NCT ID: NCT01962792 Completed - Multiple Myeloma Clinical Trials

Study of BTK Inhibitor, Ibrutinib in Combination With Carfilzomib in Subjects With Relapsed and Refractory Multiple Myeloma

Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

A MULTICENTER PHASE 1/2B STUDY OF THE BRUTON'S TYROSINE KINASE INHIBITOR, IBRUTINIB (PCI-32765), IN COMBINATION WITH CARFILZOMIB (KYPROLIS™) IN SUBJECTS WITH RELAPSED OR RELAPSED AND REFRACTORY MULTIPLE MYELOMA

NCT ID: NCT01962766 Completed - Mouth Breathing Clinical Trials

Myofunctionnal Therapy on Nasal Breathing and Orthodontic Corrections Stability

Start date: October 2013
Phase: N/A
Study type: Interventional

The current research project aims to study the efficacy of myofunctional therapy and its orthodontic long-term outcomes.

NCT ID: NCT01962168 Completed - Neoplasms Clinical Trials

Evolution® Biliary Stent System Clinical Study

Start date: December 2013
Phase: N/A
Study type: Observational

The Evolution® Biliary Stent System Clinical Study is a clinical trial on a commercially available device to gather physician experience with the Cook Evolution® Biliary Stent System for the palliation of cancer in the biliary tree. Patients will be treated as per usual medical practices.

NCT ID: NCT01962103 Completed - Cancer Clinical Trials

Study to Find a Safe Dose and Show Early Clinical Activity of Weekly Nab-paclitaxel in Pediatric Patients With Recurrent/ Refractory Solid Tumors

Start date: December 4, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find the safe dose of nab-paclitaxel in children with solid tumors, and to see if it works to treat these solid tumors in children and young adults (in Phase 1 ≤ 18 years old and in Phase 2 ≤ 24 years old). After the final dose has been chosen, patients will be enrolled according to the specific solid tumor type, (neuroblastoma, rhabdomyosarcoma, or Ewing's sarcoma), to see how nab-paclitaxel works in treating these tumors.

NCT ID: NCT01962025 Completed - Renal Failure Clinical Trials

Buttonhole Versus Step Ladder Cannulation in High Dose Hemodialysis

Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of the pilot study is to determine: 1) Will patients agree to be randomized to two different methods of putting needles in their arteriovenous fistula and, 2) if we can adequately coordinate all of the sites to get useful multicentre trial data

NCT ID: NCT01960881 Completed - Prostate Cancer Clinical Trials

Evaluation of Diet and Exercise in Prostate Cancer Patients

CRONOS II
Start date: September 19, 2013
Phase:
Study type: Observational

Canadian Real Life Evaluation of the Effect of Diet and Exercise in Prostate Cancer Patients Managed with Lupron.

NCT ID: NCT01960660 Completed - Clinical trials for Comparative Bioavailability

A Marketing-oriented Study to Evaluate the Comparative Bioavailability of Omega-3 Fatty Acids From Four Different Natural Health Products

Start date: May 2012
Phase: N/A
Study type: Interventional

Supplementation with omega-3 fatty acids has been extensively researched and is known to provide healthful benefits for patients with a diversity of conditions and diseases. Not all omega-3 supplements are created equally however; some sources of omega-3 fatty acids are superior to others due to a greater bioavailability of omega-3 fatty acids than others, differences in source material, and processing techniques. The purpose of this study is to determine which marketed omega-3 product provided the greatest effect, as measured against its' label claim and recommended dosage.

NCT ID: NCT01960439 Completed - Ulcerative Colitis Clinical Trials

Responsiveness of Endoscopic Evaluation in UC

Start date: July 2013
Phase: N/A
Study type: Observational

The purpose of this study of this study is to assess the responsiveness and validity of CIMS (Central Image Management System)-based endoscopic evaluation of UC (Ulcerative Colitis) clinical disease activity by measuring: The responsiveness central reader endoscopic EIs [(Endoscopic Indices) (MMCS (Modified Mayo Clinic endoscopy Subscore), UCEIS (Ulcerative Colitis Endoscopic Index of Severity) MBS (Modified Baron Score)] to clinical change from baseline to week 6 in a prospective trial of a treatment of known efficacy in UC.