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NCT ID: NCT01020201 Completed - Anesthesia, General Clinical Trials

Risk Factors for Post Operative Nausea and Vomiting(PONV) in Patients Underwent Gynecological Operation Under General Anesthesia

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

Risk factors for postoperative nausea and vomiting(PONV) such as past history of PONV and/or motion sickness, non-smoking status, female gender, planned opiate use for post-operative analgesia were identified in white people. Whereas, risk factors for PONV in female patient with mongolian race were not clear. As a different life style and genetic background, new risk factors may associate with PONV in this population. The present study is a prospective cohort study to identify risk factors for PONV within 24 postoperative hours in chinese female patients underwent gynecology operative under general anesthesia.

NCT ID: NCT00960180 Completed - Adult Clinical Trials

Study Evaluating Single Ascending Doses of MR1817

Start date: July 2010
Phase: Phase 1
Study type: Interventional

This is a first-in-human study of MR1817. This study will provide an initial assessment of the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of MR1817 after administration of ascending single oral doses to healthy adult subjects.

NCT ID: NCT00578526 Completed - Bladder Cancer Clinical Trials

SU011248 for Platinum-Refractory Urothelial Cancer Evaluation Trial

SPRUCE
Start date: April 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out if SU011248 works and if it is safe in patients with advanced transitional cell carcinoma.

NCT ID: NCT00519298 Completed - Healthy Clinical Trials

Study Evaluating Effects of SAM-531 on Sleep Electroencephalogram (EEG) and Quantitative Wake EEG in Healthy Subjects

Start date: October 2007
Phase: Phase 1
Study type: Interventional

Primary: To evaluate the pharmacologic effect of single doses of SAM-531 on sleep EEG in healthy subjects.

NCT ID: NCT00478829 Completed - Adult Clinical Trials

Prevalence of Depression and Anxiety in Patients Seeking Medical Care at General Health Care Settings in China

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

Objectives: Primary: To estimate the prevalence of depression and/or anxiety disorder in outpatients attending the general health care settings in China. Secondary: - To estimate gender- and age-specific prevalence of depression and/or anxiety disorder in outpatients attending the general health care settings in China. - To estimate the prevalence of depression and/or anxiety disorder in outpatients attending the general health care settings such as departments of neurology, gastroenterology, cardiology, and gynecology. - To describe the recognition and treatment rate by treating physicians as depression and/or anxiety for outpatients in the general health care settings in China.

NCT ID: NCT00387491 Completed - Adult Clinical Trials

Dose Ranging Study in Healthy Methadone Maintenance Subjects

Start date: June 2006
Phase: Phase 1
Study type: Interventional

To assess the effect of a single oral dose of MOA-728, an investigational drug, on the oral-cecal transit time in subjects who are taking methadone.

NCT ID: NCT00052273 Completed - Solid Tumor Clinical Trials

LY317615 Plus Capecitabine in Treating Patients With Advanced Solid Tumors

Start date: December 2002
Phase: Phase 1
Study type: Interventional

RATIONALE: LY317615 may stop the growth of cancer cells by blocking the enzymes necessary for cancer cell growth and by stopping blood flow to the tumor. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining LY317615 with capecitabine may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of combining LY317615 with capecitabine in treating patients who have advanced solid tumors.