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Vomiting clinical trials

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NCT ID: NCT00761254 Terminated - Nausea Clinical Trials

Domperidone for Relief of Gastrointestinal Disorders

Start date: August 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to make Domperidone available to patients with gastrointestinal disorders who have failed standard therapy and who might benefit from it.

NCT ID: NCT00757822 Active, not recruiting - Clinical trials for Postoperative Nausea and Vomiting

Prevention of Postoperative Nausea and Vomiting in Surgical Patients

PONV
Start date: December 2009
Phase: N/A
Study type: Interventional

This study will examine two different drug regimens for prevention of post-operative nausea.

NCT ID: NCT00754286 Completed - Lymphoma Clinical Trials

A Randomized Trial of The Effectiveness of Aromatherapy on Chemotherapy Induced Nausea and Vomiting in Children With Cancer

Start date: July 2008
Phase: N/A
Study type: Interventional

Aromatherapy has anecdotally been reported to decrease nausea and vomiting, decrease anxiety and increase quality of life in cancer patients. Therefore, the proposed study aims to assess the effectiveness of aromatherapy versus placebo on nausea, vomiting, anxiety and quality of life among pediatric oncology patients receiving emetogenic chemotherapy.

NCT ID: NCT00743665 Completed - Vomiting Syndrome Clinical Trials

Quality of Life And Psychological Symptoms In Children With Cyclic Vomiting Syndrome (CVS)

Start date: June 2007
Phase:
Study type: Observational

The primary aim of this study is to characterize the quality of life of youth with Cyclic Vomiting Syndrome (CVS) as well as the strategies they use to cope with stress, their strengths and vulnerabilities, and to assess symptoms of depression and anxiety in these at risk youth. The impact of CVS on the child's parent and family will also be assessed. A second aim is to evaluate the associations among coping strategies, personal strengths and vulnerabilities and the frequency and intensity of CVS attacks to determine if particular coping styles and personal characteristics are associated illness severity, psychiatric co-morbidity and quality of life

NCT ID: NCT00734929 Completed - Clinical trials for Postoperative Nausea and Vomiting

Aprepitant With Dexamethasone Versus Ondansetron With Dexamethasone for PONV Prophylaxis in Patients Having Craniotomy

Start date: September 2007
Phase: Phase 4
Study type: Interventional

We hypothesize that the combination of aprepitant with dexamethasone will provide significantly improved prophylaxis against Postoperative nausea and vomiting compared with the combination of ondansetron and dexamethasone, in patients undergoing craniotomy under general anesthesia.

NCT ID: NCT00729677 Completed - Colorectal Cancer Clinical Trials

Delayed Nausea and Vomiting in Patients With Colorectal Cancer Receiving Oxaliplatin

Start date: June 2005
Phase: N/A
Study type: Observational

RATIONALE: Learning how often patients experience nausea and vomiting after receiving anti-vomiting medicine and chemotherapy for colorectal cancer may help doctors plan better treatment and improve patients' quality of life. PURPOSE: This clinical trial is studying delayed nausea and vomiting in patients with colorectal cancer receiving standard anti-vomiting medicine during the first course of chemotherapy.

NCT ID: NCT00728104 Withdrawn - Clinical trials for Cyclic Vomiting Syndrome

The Use of L-Carnitine And CoQ10 Supplements In the Treatment of Cyclic Vomiting Syndrome (CVS)

Start date: October 2007
Phase: N/A
Study type: Observational

This is a study with the principle goal being to learn about the use of L-Carnitine and CoQ10, two vitamin supplements that are currently being used to treat Cyclic Vomiting Syndrome, largely initiated by parents. We want to learn how effective these supplements are compared to standard treatment, at what dose, and what onset of action in order to initiate future prospective study on these supplements.

NCT ID: NCT00728039 Completed - Vomiting Syndrome Clinical Trials

Quality of Life (QOL), Coping and Psychological Symptoms in Children and Adolescents With Cyclic Vomiting Syndrome

Start date: April 2007
Phase: N/A
Study type: Observational

1. Characterize the quality of life of young children with CVS (i.e., psychological, social, physical, school functioning) and the impact of the child's illness on the parent's and family's quality of life (i.e., emotional, social, cognitive functioning, communication, worry, daily activities and family relationships). 2. Assess symptoms of depression, anxiety, ADHD and behavioral problems in what our preliminary data suggests is a psychiatrically vulnerable population. 3. Evaluate the associations between quality of life and psychiatric symptoms and the frequency and intensity of CVS attacks. 4. Use the data generated from this study to develop a psychosocial intervention targeted at young children with CVS and their families who evidence risk for functional disability, with the aim of intervening as early as possible to limit the psychological and social morbidity experienced by children with CVS and their and families.

NCT ID: NCT00728026 Completed - Clinical trials for Irritable Bowel Syndrome

Autonomic Profiles in Pediatric Patients With Cyclic Vomiting Syndrome (CVS), Irritable Bowel Syndrome (IBS),Postural Orthostatic Tachycardia Syndrome (POTS), Functional Abdominal Pain (FAP) or Chronic Nausea

Start date: June 2008
Phase: N/A
Study type: Observational

Retrospectively review the charts of all children who had heart rate variability, deep breathing test, valsalva maneuver, tilt table test, thermoregulatory sweat testing, quantitative sudomotor axon reflex test (QSART) completed and were cared for at Children's Hospital of Wisconsin.

NCT ID: NCT00727974 Completed - Vomiting Clinical Trials

Genetic Analysis of Children With Cyclic Vomiting Syndrome (CVS) and Migraines

Start date: March 5, 2008
Phase:
Study type: Observational

The purpose of this study is to determine if there are genetic variations that can explain a genetic basis for cyclic vomiting syndrome (CVS).