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NCT ID: NCT01107158 Terminated - Dystocia Clinical Trials

LXRs, Cholesterol Metabolism and Uterine Dystocia

Start date: April 2010
Phase: N/A
Study type: Observational

Despite the fact that a link between cholesterol and the myometrium has been clearly established, no study investigating aspects of cholesterol metabolism and uterine dystocia currently exists. This study is a pilot study whose aim is to test the hypothesis that an association between uterine dystocia and single-nucleotide polymorphisms (SNPs) in the genes coding for the LXRs.

NCT ID: NCT01105325 Terminated - Clinical trials for Acute Coronary Syndrome

Evaluation of Compliance With Management of Acute Coronary Syndrome on Discharge From Cardiac Intensive Care

SCAVANCE
Start date: April 2010
Phase: N/A
Study type: Observational

To study compliance with secondary prevention during the first months following discharge from the cardiac intensive care unit (CIC) of patients experiencing a first episode of acute coronary syndrome : quantitative compliance over 3 months with the two principal treatments of the prescription (a statin - rosuvastatin, Crestor® and a platelet aggregation inhibitor - clopidogrel, Plavix®), using an electronic measure system ("intelligent blister" pack®);

NCT ID: NCT01105260 Terminated - Clinical trials for Spinal Cord Injuries

Effects of an Early Wheelchair Reconditionong Program on Functional Independence in Spinal Cord-inured Individuals

Start date: March 2010
Phase: N/A
Study type: Observational

Reconditioning program during the chronic phase of the spinal cord-injury is well known for its beneficial effects, but there is no investigation in early rehabilitation consequences. Nevertheless, it may be justified : to increase oxygen uptake; to decrease the risks of medical complications; or to improve the mobility. The restrictive autonomy is due to different factors: firstly wheelchair users reduce their movement because they need technical or human help to achieve transfers; and secondly, locomotion is performed by the upper limbs. Without specific practice, the upper limbs mechanical and physiological properties do not permit exercises that are long and intense. Then, the purpose of this research is to evaluate the effects of an 8 weeks interval training program on wheelchair independance during inpatient early rehabilitation for spinal cord injury (3 to 6 months post injury) compared to a control group (classical rehabilitation program in a physical medicine and rehabilitation department).

NCT ID: NCT01104506 Terminated - Clinical trials for Painful Avulsion of Brachial Plexus

Elaboration of a Pre-surgery Mapping Protocol of Primary Motor Cortex, Prior to an Implementation of a Stimulation of Primary Motor Cortex for Patients With Deafferentiation of Brachial Plexus Pain

CCPB
Start date: April 2010
Phase: N/A
Study type: Interventional

In the context of an insufficiency of clinical results for cortical stimulation in treatment of brachial plexus post-avulsion pains, one of the possibility for failure is the bad pre-surgery mapping of the area to stimulated bu the usual methods (PEM et fMRI). This purpose of this study is to realise a precise mapping of the primary motor cortex post brachial plexus avulsion. The principal endpoints is to identify and test the reliability of a muscular marker for which the cortical representation is localized immediately next to the superior member area. Several muscles of cephalic, cervical and chest area will be investigate. The methods used will be mono-shock transcranial magnetic stimulation (mTMS) and functional MRI. Concerning mTMS, several methods will be tested: best position on the scalp, realisation of outputs maps with extreme points average method, with mass center method. Concerning fMRI studies, the above paradigms will be checked: imaginary movements of hand, blow up and down abdomen, eyes winking. Statistical tests will confirm the best muscle candidate and will permit to evaluate the reliability of the method.

NCT ID: NCT01101906 Terminated - Clinical trials for Advanced Hepatocellular Carcinoma (HCC)

A Randomized, Placebo-controlled, Double-blind Phase 2 Study With OSI-906 in Patients With Advanced HCC

Start date: January 10, 2011
Phase: Phase 2
Study type: Interventional

This is a randomized, placebo-controlled, double-blind phase 2 study of OSI-906 or placebo at a continuous 150 mg twice daily (BID) dose.

NCT ID: NCT01101100 Terminated - Psoriasis Clinical Trials

Study to Assess the Long-term Safety, Tolerability, and Efficacy of AMG 827 in Subjects With Psoriasis

Start date: April 2010
Phase: Phase 2
Study type: Interventional

This study is an open-label extension of study 20090062 to evaluate extended subcutaneous dosing.

NCT ID: NCT01100879 Terminated - Clinical trials for Iron-Deficiency Anemia

Ferric Carboxymaltose for Treatment of Anaemia of Cancer in Subjects With Multiple Myeloma Receiving Chemotherapy

AOC-MM
Start date: March 2010
Phase: Phase 4
Study type: Interventional

Multicentre, randomised, controlled, 2-arm open-label prospective pilot study to evaluate efficacy and safety of ferric carboxymaltose (FCM) in treatment of anaemia in subjects with multiple myeloma (MM) initiating chemotherapy. The subjects will be screened for eligibility within 4 weeks prior to inclusion and randomised to receive intravenous infusions of FCM or standard care (the subjects may be treated according to the local institutional practice if requiring symptomatic management of anaemia). Thereafter the visits are scheduled at Weeks 0, 2, 4, 6 and 8.

NCT ID: NCT01100515 Terminated - Clinical trials for Carbon Monoxide Poisoning

Hyperbaric Oxygen Therapy for Acute Domestic Carbon Monoxide (CO) Poisoning

Start date: October 1989
Phase: Phase 3
Study type: Interventional

Carbon monoxide poisoning still places a burden on the healthcare system worldwide. While oxygen therapy is the cornerstone treatment, the role and practical modalities of hyperbaric oxygen therapy (HBO) remain controversial. This study aimed at comparing one session of HBO at 2 absolute atmosphere followed by 4 hours of normobaric oxygen therapy to 6 hours of normobaric oxygen therapy in adult victims of acute domestic carbon monoxide poisoning and without coma.

NCT ID: NCT01100190 Terminated - Clinical trials for Ptosis of the Neck, Mid-face and/or Jowl

A Prospective Study of the NUVANCE Facial Rejuvenation System for Mid-Face, Neck and Jowl Rejuvenation Procedures

Start date: March 1, 2010
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the clinical tolerability of the NUVANCEā„¢ Facial Rejuvenation System for correcting neck, mid-face and/or jowl ptosis.

NCT ID: NCT01099995 Terminated - Clinical trials for Carbon Monoxide Poisoning

Hyperbaric Oxygen Therapy for Comatose Patients With Acute Carbon Monoxide Poisoning

Start date: October 1989
Phase: Phase 3
Study type: Interventional

Carbon monoxide poisoning still places a burden on the healthcare system worldwide. While oxygen therapy is the cornerstone treatment, the role and practical modalities of hyperbaric oxygen therapy (HBO) remain controversial. This study aimed at comparing two sessions of HBO at 2 absolute atmosphere and one session of HBO at 2 absolute atmosphere followed by 4 hours of normobaric oxygen therapy in comatose adult victims of acute domestic carbon monoxide poisoning.