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NCT ID: NCT01252589 Completed - Clinical trials for Chronic Myeloid Leukemia

Patient Reported Outcomes in Chronic Myeloid Leukemia

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

Although the impact of disease and treatment related burden on health-related quality of life (HRQOL) in patients with solid tumours has been well studied, with several clinical trials that included HRQOL as an endpoint, the general understanding in patients with Chronic Myeloid Leukaemia (CML) is lacking in comparison. The literature shows that patients' perspective is unique and should always be measured with methodologically sound instruments that are devised for this purpose. The main scope of this project is develop to an international validated questionnaire for the purpose of HRQOL assessment; such a tool will then be used to provide important data, from the patients' perspective, to make more informed treatment decisions.

NCT ID: NCT01177072 Completed - Depression Clinical Trials

Study of Effectiveness of Mental Health Interventions Among Torture Survivors in Southern Iraq

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

1. That the psychotherapeutic intervention - Components-Base Interventions (CBI) - is effective in reducing the severity of mental health symptoms experienced by torture survivors in Southern Iraq. 2. That the psychotherapeutic intervention - Cognitive Processing Therapy (CPT) - is effective in reducing the severity of mental health symptoms experienced by torture survivors in Southern Iraq.

NCT ID: NCT00925262 Completed - Depression Clinical Trials

Controlled Trial of Mental Health Interventions for Torture Survivors in Kurdistan

Start date: June 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the relative effectiveness of three different mental health counseling interventions in the treatment of mental health problems commonly affecting torture and trauma survivors living in Kurdistan, Iraq.

NCT ID: NCT00892229 Completed - Missed Abortion Clinical Trials

Buccal Versus Vaginal Misoprostol in Surgical Termination of the First Trimester Missed Abortion in Erbil

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effectiveness of buccal misoprostol and comparing this with vaginal route of the same drug.

NCT ID: NCT00822263 Completed - Clinical trials for Mild Traumatic Brain Injury

The Use of Anti-oxidants to Reduce Sequela of Mild Traumatic Brain Injury (mTBI) After Blast Exposure

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

The administration of N-acetyl-cysteine (an anti-oxidant) for seven days along with observation will result in improved hearing and balance function in individuals who demonstrate these disorders after blast exposure when compared to a placebo medicine and observation at the seven day time point.

NCT ID: NCT00797693 Completed - Miscarriage Clinical Trials

Misoprostol in Termination of First Trimester Missed Abortion

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

The purpose of this study is to determine whether oral versus vaginal misoprostol is effective in termination of first trimester missed abortion and to compare between two different routes.

NCT ID: NCT00517166 Completed - Vascular Injury Clinical Trials

Survey of Tourniquet Use in a Combat Support Hospital

Start date: August 2006
Phase: N/A
Study type: Observational

Data will be collected on the type of tourniquet and circumstances of its use. Patients with penetrating extremity injury will have clinical and pre-clinical hospital data collected.