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NCT ID: NCT00749294 Completed - Warts Clinical Trials

Anogenital Wart Burden and Cost of Illnesses

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

The study will be a prospective study of patients presenting with anogenital warts. The objective are to assess proportion of anogenital warts to the total number of sexual transmitted infection patients, to quantify direct and indirect cost of illnesses and psychological burden associated with anogenital warts and to estimate government program expenditure for the prevention and control and treatment of the STI/anogenital HPV infection.

NCT ID: NCT00748462 Completed - Acne Scar, Wrinkle Clinical Trials

Fractional CO2 Treatment of Acne Scars in Asians

CO2
Start date: July 2008
Phase: Phase 4
Study type: Interventional

The objective of this study is to investigate the efficacy and side effects of a fractional CO2 laser for treatment of acne scar in Asians.

NCT ID: NCT00746551 Completed - Anemia Clinical Trials

Intravenous Versus Oral Iron in Late Pregnancy: Results of Treatment

EIVF
Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy of body iron storage replenishment between low dose intravenous iron and oral iron in late pregnancy.

NCT ID: NCT00746538 Recruiting - Clinical trials for Unresectable Hilar Cholangiocarcinoma

Quality of Life in Patients With Unresectable Hilar Cholangiocarcinoma on Palliative Metallic Stent Versus Plastic Stent

Start date: January 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the quality of life in patients with unresectable hilar cholangiocarcinoma on palliative metallic stent versus plastic Stent.

NCT ID: NCT00741832 Unknown status - Clinical trials for Chronic Obstructive Pulmonary Disease

The Effects of a Positive Expiratory Pressure (PEP) on Dyspnea and Dynamic Hyperinflation During Exercise in Chronic Obstructive Pulmonary Disease (COPD) Patients

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

From the relationship between pathophysiology of chronic obstructive pulmonary disease (COPD), dyspnea, and dynamic hyperinflation during ventilatory increasing, the investigators hypothesize that 1. Positive expiratory pressure (PEP) breathing will reduce dyspnea more than normal breathing during exercise in mild to moderate COPD patients. 2. PEP breathing will improve dynamic hyperinflation during exercise more than normal breathing in mild to moderate COPD patients. 3. PEP breathing will improve cardiorespiratory function during exercise than normal breathing in mild to moderate COPD patients.

NCT ID: NCT00741637 Completed - Diarrhea Clinical Trials

Safety and Immunogenicity of Single Dose Choleragarde® in HIV-Seropositive Adults

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

The purpose of this study is to assess the safety and immunogenicity of Peru-15 (CholeraGarde®) vaccine in HIV seropositive adult population of Bangkok Thailand

NCT ID: NCT00741533 Completed - Quality of Life Clinical Trials

Quality of Life in Thai Women Diagnosed Cervical Cancer at King Chulalongkorn Memorial Hospital

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

To study the quality of life of patients earlier diagnosed for cervical cancer and cervical intraepithelial neoplasia (CIN).

NCT ID: NCT00740142 Completed - Clinical trials for Hepatic Encephalopathy

Efficacy of Combined Oral L-ornithine-L-aspartate and Lactulose in Patients With Hepatic Encephalopathy

Start date: September 2008
Phase: Phase 4
Study type: Interventional

Hypothesis: Is the combination of oral L-ornithine-L-aspartate and lactulose more efficacious than oral lactulose alone in treatment of hepatic encephalopathy? Study design; Randomized, double-blinded, placebo controlled trial

NCT ID: NCT00737308 Completed - Clinical trials for Dental Restoration Wear

Properties and Clinical Performance of Zirconia-based Dental Ceramics

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

The objectives of this study are to determine the clinical performance of zirconia-based dental prostheses and their related properties.

NCT ID: NCT00736099 Completed - Clinical trials for Diabetes Mellitus, Type 2

Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM

Start date: August 2008
Phase: Phase 3
Study type: Interventional

The objective of the current study is to investigate the safety and tolerability of BI 1356 (5 mg / once daily) given for 78 weeks in different modalities of treatment. The treatment modalities are determined by the treatment in the blinded trial in which every patient was included previously as BI 1356 in monotherapy (patients in 1218.16 trial), BI 1356 in combination with pioglitazone (patients in 1218.15 trial), BI 1356 added to metformin background (patients in 1218.17 trial) or BI 1356 added to a background therapy of metformin in combination with a sulphonylurea (patients in 1218.18 study)