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NCT ID: NCT01554111 Completed - Cathartic Colon Clinical Trials

Comparing Bowel Preparation Regimens for Flexible Sigmoidoscopy

Start date: March 2012
Phase: Phase 4
Study type: Interventional

Objective and Hypothesis: The investigators objective is to help determine the efficacy of oral and rectal bowel preparation regimens for sigmoidoscopy. The investigators hypothesis is that oral preparation will reduce the amount of repeat rectal enemas required and improve the quality of a bowel exam at the sigmoidoscopy.

NCT ID: NCT01553747 Completed - Clinical trials for Irritable Bowel Syndrome

Efficacy, Safety, and Tolerability of Eluxadoline in the Treatment of Participants With Diarrhea-Predominant Irritable Bowel Syndrome (IBS-d)

Start date: May 29, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the efficacy, safety, and tolerability of different doses of eluxadoline (JNJ-27018966) compared with placebo in the treatment of participants with diarrhea-predominant irritable bowel syndrome.

NCT ID: NCT01553617 Completed - Clinical trials for Heart; Dysfunction Postoperative, Cardiac Surgery

VolulyteTM in Cardiac Surgery

Start date: October 2012
Phase: Phase 4
Study type: Interventional

The study will compare the efficacy and safety of VolulyteTM and human albumin in elective open-heart surgery in adult patients.

NCT ID: NCT01553591 Completed - Clinical trials for Irritable Bowel Syndrome

Efficacy, Safety, and Tolerability of Eluxadoline in the Treatment of Participants With Diarrhea-Predominant Irritable Bowel Syndrome (IBS-d)

Start date: May 29, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the efficacy, safety, and tolerability of different doses of eluxadoline (JNJ-27018966) compared with placebo in the treatment of participants with diarrhea-predominant irritable bowel syndrome.

NCT ID: NCT01553292 Completed - Clinical trials for Respiratory Distress Syndrome

Early CPAP And Large Volume Minimally Invasive Surfactant (ECALMIST) in Preterm Infants With RDS

ECALMIST
Start date: April 2012
Phase: N/A
Study type: Interventional

Modification of Minimally Invasive Surfactant Therapy (MIST) to a new technique called ECALMIST (Early CPAP And Large volume Minimal Invasive Surfactant). This modification is needed to adapt the use of large volume surfactant of 4-5 ml/kg. The ECALMIST will be used to deliver the large volume Surfactant that been used in Canada called BLES (about 5 ml for each 100 mg) to the preterm infants bellow 35 weeks gestation suffer from respiratory distress syndrome (RDS) in 1st 24 hours of life while maintained on CPAP.

NCT ID: NCT01553149 Completed - Clinical trials for Neurofibromatosis Type 1

Low-Dose or High-Dose Lenalidomide in Treating Younger Patients With Recurrent, Refractory, or Progressive Pilocytic Astrocytoma or Optic Pathway Glioma

Start date: July 5, 2012
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well low-dose lenalidomide works compared with high-dose lenalidomide in treating younger patients with juvenile pilocytic astrocytomas or optic nerve pathway gliomas that have come back (recurrent), have not responded to treatment (refractory), or are growing, spreading, or getting worse (progressive). Lenalidomide is classified as an immunomodulatory drug as it boosts the immune system. It has other potential anti-tumor effects, for example, it may stop the growth of tumor cells by blocking blood flow to the tumor. It is not yet known whether low-dose lenalidomide is more or less effective than high-dose lenalidomide in treating patients with juvenile pilocytic astrocytomas or optic nerve pathway gliomas.

NCT ID: NCT01552902 Completed - Clinical trials for Attention-deficit/Hyperactivity Disorder

Effectiveness of Vyvanse Compared to Concerta in Adolescents With Attention-deficit/Hyperactivity Disorder

Start date: April 3, 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine effectiveness of Vyvanse compared to Concerta in adolescents with Attention-deficit/Hyperactivity Disorder (ADHD).

NCT ID: NCT01552304 Completed - Clinical trials for Obstructive Sleep Apnea

Oxygen Supplementation Study in Obstructive Sleep Apnea (OSA) Patients

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

Hypotheses: 1. Postoperative oxygen therapy significantly improves postoperative oxygenation in OSA surgical patients. 2. Postoperative oxygen therapy do not significantly increase the number of apnea episodes and the duration of apnea episodes. 3. Postoperative oxygen therapy do not significantly increase arterial carbon dioxide(CO2) level in OSA surgical patients.

NCT ID: NCT01551706 Completed - Oxidized LDL Level Clinical Trials

Pilot Study to Evaluate the Effect of ENI Patented Whole Grape Extract on Antioxidant Status

Start date: February 2012
Phase: Phase 1
Study type: Interventional

This is a Randomized, Double-blind, Placebo-controlled, Pilot Study to Evaluate the Effect of ENI Patented Whole Grape Extract on Antioxidant Status.

NCT ID: NCT01551147 Completed - Asthma Clinical Trials

A Placebo and Active Controlled Study of ONO-6950 Following Allergen Challenge in Patients With Asthma

Start date: June 2012
Phase: Phase 2
Study type: Interventional

The primary objectives are - to determine the effect of ONO-6950 200 mg QD versus placebo administered for 8 days on early asthmatic response (EAR) and late asthmatic response (LAR) induced by inhaled allergen - to determine the safety and tolerability of ONO-6950 200 mg QD administered for 8 days in patients with asthma The secondary objectives are: - to compare the effect of ONO-6950 versus montelukast on the % decrease of FEV1 following allergen exposure, and - to determine the effect of ONO-6950 versus placebo and montelukast on allergen-induced airway hyperresponsiveness (AHR) as measured by methacholine challenge