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NCT ID: NCT02648919 Terminated - Prostate Cancer Clinical Trials

Clinical Study of Noni Extract in Men With Very Low Risk or Low Risk Prostate Cancer

Start date: December 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effects of Noni extract in men diagnosed with very low risk or low risk prostate cancer

NCT ID: NCT02648867 Terminated - Clinical trials for Prolonged Second Stage of Labor

Evaluation of Maternal Feedback to Shorten Pushing Efforts During Labor

Start date: December 2015
Phase: N/A
Study type: Interventional

This study will assess the ability for continuous electronic feedback to reduce the length of second stage labor and improve maternal and fetal outcomes.

NCT ID: NCT02648711 Terminated - Solid Tumors Clinical Trials

Alternative Dosing for CRLX101(NLG207) Alone, With Avastin and With mFOLFOX6 in Advanced Solid Tumors

Start date: October 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of weekly dosing of CRLX101 (both as monotherapy; (Schedule 1) and in combination with bevacizumab every 2 weeks (Schedule 2) and weekly with a 3 week on / 1 week off schedule in combination with mFOLFOX6 (Schedule 3) to affirm the dose for future clinical studies.

NCT ID: NCT02648633 Terminated - Glioblastoma Clinical Trials

Stereotactic Radiosurgery With Nivolumab and Valproate in Patients With Recurrent Glioblastoma

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

The purpose of this study is to evaluate the safety and feasibility of the immunotherapeutic agent nivolumab given in combination with gamma knife therapy and valproate in patients with recurrent glioblastoma, a common and lethal type of brain cancer.

NCT ID: NCT02647892 Terminated - Local Anesthesia Clinical Trials

Optimal Lidocaine Buffering to Reduce Injection Pain in Local Anesthesia

Start date: January 8, 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the optimal amount of lidocaine buffering needed to decrease injection pain when administering local anesthesia.

NCT ID: NCT02647645 Terminated - HIV Clinical Trials

Cognitive Training With and Without tDCS to Improve Cognition in HIV

Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to develop pilot data on the potential efficacy of computer-based cognitive training or the combination of computer-based cognitive training with transcranial direct current stimulation (tDCS) in improving cognitive function in persons with HIV-related mild neurocognitive disorder (MND).

NCT ID: NCT02644122 Terminated - Clinical trials for Metastatic Squamous Neck Cancer With Occult Primary Squamous Cell Carcinoma

SF1126 in Recurrent or Progressive SCCHN and Mutations in PIK3CA Gene and/or PI-3 Kinase Pathway Genes

Start date: November 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test the good and bad effects of an experimental drug called SF1126. This drug is being tested in patients whose cancer has not been controlled by available standard therapies and who have certain genes in their tumor. SF1126 is a drug that inhibits a cell protein called phosphatidyl inositol 3 kinase (PI3K). PI3K is part of signaling pathway that tells cancer cells to grow, survive, invade and metastasize. PI3K also has an important role in the development of blood vessels that are required to support tumor growth. SF1126 is being developed by SignalRx Pharmaceuticals, Inc. It is considered an experimental drug because it is not approved by the FDA for any disease treatment.

NCT ID: NCT02644083 Terminated - Multiple Sclerosis Clinical Trials

Tecfidera and MRI for Brain Energy in MS

Start date: February 2016
Phase:
Study type: Observational

The primary objective of this study is to test the hypothesis that DMF can improve mitochondrial function in the brain of people with MS. The investigators will assess mitochondrial function in the cerebral grey matter by measuring PCr and ATP by 31P magnetic resonance spectroscopy (MRS) and NAA in NAWM by 1H MRS.

NCT ID: NCT02643979 Terminated - Obesity Clinical Trials

Ketamine and Propofol Combination Versus Propofol for Upper Gastrointestinal Endoscopy

Start date: January 1, 2016
Phase: Phase 4
Study type: Interventional

Propofol is one of the most popular anesthetic drugs used for sedation during upper gastrointestinal endoscopies due to its quick onset and quick resolution of symptoms allowing patients to leave the hospital sooner. However, when administered it can also slow the breathing of patients and cause others to have upper airway obstruction (such as snoring) which can impede proper spontaneous breathing. Ketamine is an agent that is capable of providing both pain control and sedation while having either minimal effect on breathing or promoting spontaneous breathing. Combining Ketamine with Propofol has the potential to reduce the total amount of Propofol used resulting in a procedure being performed under the same level of sedation but without the downside of reduced spontaneous breathing. Patients who are obese (defined as body mass index greater than 35) tend to be even more susceptible to this effect of Propofol. The researchers are investigating whether the addition of Ketamine will indeed allow for this continued comfortable level of sedation while promoting continued spontaneous breathing in obese patients undergoing upper gastrointestinal endoscopies.

NCT ID: NCT02643524 Terminated - Foot Injury Clinical Trials

Weight Change With Controlled Ankle Movement (CAM) Walker Boot Use

Start date: December 7, 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if patients wearing a CAM walker boot have a change in weight compared to patients who wear a CAM boot and are provided nutritional and upper body exercise information.