Clinical Trials Logo

Syndrome clinical trials

View clinical trials related to Syndrome.

Filter by:

NCT ID: NCT01958476 Completed - Clinical trials for Neonatal Abstinence Syndrome

Improving Outcomes in Neonatal Abstinence Syndrome

Start date: September 2013
Phase: Phase 3
Study type: Interventional

1: SPECIFIC Aim I: To compare treatment options for neonatal abstinence syndrome (NAS) due to in-utero narcotic exposure. One hundred eighty four full-term infants with a diagnosis of NAS requiring medications will be studied. Infants will be randomized to receive either morphine or methadone. It is hypothesized that morphine treated infants will do better and require fewer days in the hospital compared to methadone treated infants. 2. SPECIFIC Aim II: To evaluate the effects of NAS treatment on long-term neurodevelopmental outcome. Infants will be evaluated with development testing at 18 months of age. It is hypothesized that morphine treated infants will have better neurodevelopmental outcomes. It is also hypothesized that neurobehavioral abnormalities identified at two weeks of age will correlate with neurodevelopmental impairment at 18 months. 3: SPECIFIC Aim III: To determine if common genetic variations in the genes involving narcotic action contribute to the severity of NAS. A DNA sample will be obtained from all infants and analyzed for differences in 3 key genes. This will then be correlated with short-term and long-term outcomes.

NCT ID: NCT01958424 Completed - Metabolic Syndrome Clinical Trials

In Vitro Fertilization Outcomes in Metabolic Syndrome

Start date: April 2014
Phase: N/A
Study type: Observational

The purpose of this study is to examine the effect of metabolic syndrome in over-weight women on IVF treatment outcomes.

NCT ID: NCT01957644 Terminated - Clinical trials for Myelodysplastic Syndromes

Phase I Dose Escalation Trial of Volasertib in Combination With Azacitidine in Patients With MDS or CMML

Start date: November 6, 2013
Phase: Phase 1
Study type: Interventional

To investigate the maximum tolerated dose (MTD), safety, pharmacokinetics, and efficacy of volasertib in combination with azacitidine in patients with myelodysplastic syndromes (MDS) or chronic myelomonocytic leukemia (CMML) and not candidates for hematopoietic stem cell transplant

NCT ID: NCT01956188 Active, not recruiting - Clinical trials for Systemic Lupus Erythematosus

Omega 3 in LES and APS

Start date: May 2014
Phase: N/A
Study type: Interventional

It has been demonstrated that EPA and DHA supplementation may have anti-inflammatory properties in several chronic diseases, namely, diabetes, obesity, and in rheumatoid arthritis, although not with controversy. Systemic lupus erythematosus (SLE) and Antiphospholipid Antibody Syndrome (AAS) are autoimmune diseases characterized by a chronic inflammatory state which is associated with the disease´s clinical symptoms. Thus, we hypothesized that EPA and DHA supplementation may beneficially affect the inflammatory cytokine profile and clinical features of LES and AAS patients.

NCT ID: NCT01955525 Not yet recruiting - Clinical trials for Acute Coronary Syndrome

Long-term Follow-up of Health Related Quality of Life in Patients With Acute Coronary Syndrome

EMMACE-3X
Start date: November 2013
Phase: N/A
Study type: Observational [Patient Registry]

This study is aiming to i)measure longterm health related quality of life (HRQL) outcomes of the EMMACE3 patients hospitalised with acute coronary syndromes (ACS) and evaluate possible associations with their cardiovascular profile and to ii) Linkage these data to multiple electronic healthcare records

NCT ID: NCT01954420 Completed - Pain Clinical Trials

A Brief Patient-Controlled Intervention for a Symptom Cluster in Advanced Cancer

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

The purpose of the research is to test the efficacy of a patient-controlled cognitive-behavioral intervention for pain, fatigue, and sleep disturbance during cancer treatment, and to evaluate moderators and mediators of intervention effects. The intervention uses guided imagery, relaxation exercises, and nature sound recordings, self-administered via an MP3 player. The study will determine (1) if the intervention helps to control symptoms during chemotherapy, (2) if personal and clinical characteristics influence how well the intervention works, and (3) if the cognitive-behavioral strategies reduce markers of stress and inflammation found in blood and saliva.

NCT ID: NCT01953796 Completed - Clinical trials for Polycystic Ovary Syndrome

Clomiphene Stair-Step Protocol for Ovulation Induction in Women With Polycystic Ovarian Syndrome

PCOSCCTvUSS
Start date: May 2010
Phase: N/A
Study type: Interventional

The objective of our study is to evaluate the efficacy of the clomiphene stair-step protocol to induce ovulation in women with polycystic ovarian syndrome (PCOS) compared to traditional protocol. Methods:This was a randomized controlled clinical trial at the Fertility clinic of Al sadder teaching hospital at Al- Najaf city, Iraq . It included 140 women who met all of the inclusion criteria, they were divided into two groups; 65 patients for the stair step protocol and 75 patients for the traditional protocol.

NCT ID: NCT01953276 Completed - Clinical trials for Acute Coronary Syndrome

Are Serial Electrocardiograms Additive to SeriAl Second-generations Troponins in Predicting Acute CoronAry Syndromes in PatienTs With Undifferentiated cHest Pain

ASAP Cath
Start date: January 2013
Phase:
Study type: Observational

Our research will examine whether the presence or absence of serial electrocardiogram (ECG) changes aids in reclassifying participants' risk for major adverse cardiac events (MACE) over and above serial blood testing.

NCT ID: NCT01952392 Completed - Clinical trials for Acute Coronary Syndrome

Prevention of Cardiovascular Events by Antiplatelet Agents After Acute Coronary Syndrome

AReMIS
Start date: October 2013
Phase: N/A
Study type: Observational

Prevention of cardiovascular events by antiplatelet agents after acute coronary syndrome

NCT ID: NCT01952275 Recruiting - Clinical trials for Pyoderma Gangrenosum

Observational Study of the Genetic Architecture of Neutrophil-Mediated Inflammatory Skin Diseases

NEUTROGENE
Start date: January 2014
Phase: N/A
Study type: Observational

This study investigates the genetic architecture of Neutrophil-Mediated Inflammatory Skin Diseases. After collecting informed consent, all patients' clinical phenotype is graded at inclusion with a detailed case report form and a discovery cohort formed based on the certainty of diagnosis. The DNA of patients in the discovery cohort is analyzed by whole exome sequencing which identifies all protein-coding genetic variants. Subsequently, statistical burden tests are going to identify enrichment of rare coding genetic variants in patients affected by Neutrophil-Mediated Inflammatory Skin Diseases. The ultimate goal is to reveal the responsible gene(s) that may then be targets for clinical intervention.