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NCT ID: NCT01393626 Completed - Crohn's Disease Clinical Trials

A Study To Investigate Safety And Efficacy Of CP-690,550 For Induction Therapy In Subjects With Moderate To Severe Crohn's Disease

Start date: October 2011
Phase: Phase 2
Study type: Interventional

This study investigates safety and efficacy of CP-690,550 in adult patients with moderate to severe Crohn's disease. The study hypothesis is that at least one dose of the tested drug is more effective than placebo (inactive drug).

NCT ID: NCT01393587 Not yet recruiting - Oxidative Stress Clinical Trials

A New Exogenous Marker for Diagnosis of Oxidative Stress During Laproscopic Surgery

Start date: n/a
Phase: N/A
Study type: Interventional

Recently, a new synthetic marker was developed, based on a molecule that is composed of Amino Acids and Linoleic Acid and Neucleic Acid, which is capable of detecting even minor changes of oxidative stress. The investigators would like to assess the usefulness of this marker during positive pressure pneumoperitoneum, during laproscopic surgery, with or without intenstinal resection (ischemia induced by intra-abdominal pressure and vascualr compromise).

NCT ID: NCT01393574 Recruiting - Clinical trials for Attention Deficit Hyperactivity Disorder

Comparing Treatment With Melatonin to Treatment With Stimulants (Methylphenidate) in Children With Attention Deficit Hyperactivity Disorder and Sleep Difficulties

Start date: June 2011
Phase: Phase 4
Study type: Interventional

The study hypothesis is that some children with Attention-Deficit-Hyperactivity-Disorder (ADHD) who also have sleep onset difficulties will improve with Melatonin treatment to an extent similar to that of stimulants treatment. In order to check this hypothesis children with a new ADHD diagnosis who also have sleep difficulties will be treated with either Melatonin or with stimulants (Methylphenidate) for one month. The main outcome will be improvement of the ADHD symptoms.

NCT ID: NCT01392664 Completed - Clinical trials for Urinary Stress Incontinence Treated by TVT

TVTO Versus TVTFFM for Urinary Stress Incontinence

Start date: February 2009
Phase: N/A
Study type: Observational

Women who had urinary stress incontinence and underwent one of two procedures: the classic TVTO or the Folke-Flam method of surgical operation, will be evaluated and compared.

NCT ID: NCT01392651 Completed - Clinical trials for Urinary Stress Incontinence

Tension-free-vaginal-tape-obturator (TVTO) Versus Tension-free-vaginal-tape-Secur (TVTS) for Treatment of SUI

Start date: January 2009
Phase: N/A
Study type: Observational

Women with urinary stress incontinence who underwent surgical treatment by either TVTO or TVTS will be enrolled. The investigators will collect data from charts and use a telephone questionnaire to check the outcome of these women. Physical examination findings will also be incorporated.

NCT ID: NCT01392417 Completed - Clinical trials for Pelvic Floor Prolapse

Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

Start date: February 2009
Phase: N/A
Study type: Observational

Women who had surgery for pelvic floor prolapse underwent surgery by anterior Prolift or Posterior prolift at least a year after the surgery. The data from the charts and from telephone conversations with the patients will be entered to a database. Physical examination data will also be incorporated.

NCT ID: NCT01392326 Completed - Psoriatic Arthritis Clinical Trials

Efficacy at 24 Weeks and Long Term Safety, Tolerability and Efficacy up to 2 Years of Secukinumab (AIN457) in Patients With Active Psoriatic Arthritis (PsA)

FUTURE 1
Start date: September 2011
Phase: Phase 3
Study type: Interventional

This study will assess the efficacy and safety of secukinumab in patients with active psoriatic arthritis who are intolerant to or have had an inadequate response to NSAIDs, DMARDs and / or TNFα inhibitor therapy.

NCT ID: NCT01390220 Terminated - Epilepsy Clinical Trials

Study to Evaluate the Safety and Efficacy of USL261 (Intranasal Midazolam) in Patients With Seizure Clusters

ARTEMIS1
Start date: June 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine the safety and effectiveness of USL261 for the outpatient treatment of seizure clusters.

NCT ID: NCT01389908 Recruiting - Schizophrenia Clinical Trials

A Follow up Study of Intramuscular Olanzapine Depot in Patients With Schizophrenia or Schizoaffective Disorder

Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the long-term efficacy of Olanzapine Pamoate (OP) Depot in patients diagnosed with schizophrenia or schizoaffective disorder.

NCT ID: NCT01389648 Completed - Abdominal Surgery Clinical Trials

Pre-operative Physiotherapy to Prevent Post-operative Complications

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the roll of pre-operative chest physiotherapy, in addition to the usual care given after major abdominal surgery, in the prevention of post-operative respiratory complications.