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NCT ID: NCT02114476 Active, not recruiting - Diabetes Mellitus Clinical Trials

Effect of Implantable Contraception on Type-2 DM and Metabolic Syndrome in Women With History of Gestational DM

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

The purpose of this study is to determine the effect of implantable contraception on the incidence of diabetes mellitus in women with history of gestational diabetes mellitus comparing with those using nonhormonal contraceptives.

NCT ID: NCT02112656 Completed - Clinical trials for Hepatocellular Carcinoma

Study of ThermoDox With Standardized Radiofrequency Ablation (RFA) for Treatment of Hepatocellular Carcinoma (HCC)

OPTIMA
Start date: June 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether ThermoDox, a thermally sensitive liposomal doxorubicin, is effective in the treatment of non-resectable hepatocellular carcinoma when used in conjunction with standardized radiofrequency ablation (sRFA).

NCT ID: NCT02112305 Active, not recruiting - Acute Severe Asthma Clinical Trials

Compare Efficacy Nebulized and Intravenous Magnesium Sulphate in Thai Children

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

The purpose of this study is to determine whether nebulized magnesium sulphate is effective in the treatment of acute severe asthma when comparison with intravenous magnesium sulphate

NCT ID: NCT02108327 Completed - Blood Loss Clinical Trials

Blood Loss Between Surgical Blade and Unipolar Electrocautery in TKA

TKA
Start date: April 2014
Phase: N/A
Study type: Interventional

Using of surgical blade may have less blood loss than unipolar electrocautery in Total Knee Arthroplasty (TKA).

NCT ID: NCT02108197 Completed - Clinical trials for Gestational Diabetes

Sleep Apnea and Gestational Diabetes

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

The investigators hypothesize that pregnant women with gestational diabetes will have a high incidence of sleep apnea, and that the treatment of sleep apnea will lead to improved glucose control in these women.

NCT ID: NCT02107911 Completed - HIV Clinical Trials

Factors Affecting the Intention to Take nPEP Among Thai MSM

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

The potential participants will be informed of the study details, including the study objectives. Once they have read the study information sheet and have a good understanding of the study, those who intend to participate in the study will be asked to sign the consent form for this study. There are 2 groups of participants: MSM who seek HIV voluntary counseling and testing service (phase I) and MSM who meet nPEP criteria (phase II).

NCT ID: NCT02106832 Completed - Bronchiectasis Clinical Trials

Ciprofloxacin Dry Powder for Inhalation (DPI) in Non-cystic Fibrosis Bronchiectasis (Non-CF BE)

RESPIRE 2
Start date: April 30, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate if the time to first pulmonary exacerbation of bronchiectasis or its frequency can be prolonged by inhalation of ciprofloxacin for 28 days every other 28 days or for 14 days every other 14 days over 48 weeks.

NCT ID: NCT02106793 Completed - Clinical trials for Chronic Rhinosinusitis

Mitomicin C for Prevention Postoperative Endoscopic Sinus Surgery Synechia and QOL in Chronic Rhinosinusitis

Start date: March 2015
Phase: Phase 3
Study type: Interventional

Primary objective - To compare the incidence of postoperative nasal synerchia between Mitomicin C and placebo in patients at 6 months after endoscopic sinus surgery - To validate the Thai version of disease-specific quality of life tool SNOT-22 Secondary objectives - To compare the clinical signs and symptoms of CRS in patients who receive Mitomicin C with those who receive placebo - To compare the disease-specific quality of life in patients who receive Mitomicin C with those who receive placebo - To compare the side effects of Mitomicin C versus placebo

NCT ID: NCT02106273 Completed - Clinical trials for One-lung Ventilation

The Use of LMA-Proseal and Endobronchial Blocker for One Lung Anesthesia, Case Series

Start date: April 2011
Phase: Phase 4
Study type: Observational

An observational pilot study to determine the success rate of using LMA Proseal in conjuction with endobronchial blocker to provide one-lung anesthesia for thoracic surgery.

NCT ID: NCT02105311 Completed - Clinical trials for Intraocular Pressure

Effect of Selective Laser Trabeculoplasty Versus Travoprost on Circardian Intraocular Pressure

Start date: March 2014
Phase: Phase 4
Study type: Interventional

The investigators conduct this study to access the effect of selective laser trabeculoplasty on 24-hour circadian tension curves of patients with open-angle glaucoma, normal tension glaucoma and ocular hypertension. This treatment effect is compared with that of the prostaglandin analogue, travoprost.