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NCT ID: NCT01259349 Recruiting - Cataract Clinical Trials

Effect of Minimising Ultrasound Power to 1% During Cataract Surgery on Corneal Endothelium.

OCTOPUS
Start date: November 2010
Phase: Phase 3
Study type: Interventional

Coaxial microincision cataract surgery using 1% ultrasound is not inferior to standard coaxial microincision cataract surgery in patients of grade 0.1-6.0 immature senile cataract in terms of corneal endothelial safety.

NCT ID: NCT01228786 Recruiting - Clinical trials for Primary Hyperparathyroidism (PHPT)

Regulation of Vitamin D Receptor (VDR),Calcium Sensing Receptor (CaSR), Cyclin D1,Ki67 and Proliferating Cell Nuclear Antigen (PCNA) in Primary Hyperparathyroidism

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

The present study is designed to examine the expression of VDR, CaSR, PTH, Cyclin D1, Ki67 and PCNA and to find out its relationship with clinical parameters in parathyroid adenomas. Examination of the contribution of genes expression can elucidate the critical link between proliferation and functional abnormalities in parathyroid adenomas. Alternative to DNA and RNA, protein expression can provide a better understanding of this disease.

NCT ID: NCT01212328 Recruiting - Hypertension Clinical Trials

A Multi-site, Individually Randomized, Controlled Translation Trial of Integrated and Comprehensive Care Strategies to Reduce Cardiovascular Disease (CVD) Risk Among 1,120 Type 2 Diabetes Mellitus(T2DM) Patients in South Asia

CARRS
Start date: October 2010
Phase: N/A
Study type: Interventional

Background: Cardiovascular diseases (CVD) are currently the leading cause of death globally and Asian Indians will account for between 40-60% of the global CVD burden within the next 10-15 years. Risk factor control and preventive care are effective in reducing CVD events and mortality. The greatest gains in CVD prevention have been seen when early and target-driven interventions address multiple risk factors together. However, achieving control of even individual risk factors (blood glucose, blood pressure, or blood lipid targets) is poor, globally. Quality improvement schemes, like the proposed intervention, have shown promise in high-income countries, but are untested in South Asia; a region with a population at extraordinarily high CVD risk. Objective: To test whether a clinic-based case management intervention (consisting of guidelines based treatment, care coordinator assistance and decision support software) to reduce cardiovascular disease (CVD) risk among Type 2 diabetes patients in South Asia, is more effective and sustainable compared to existing care. Trial subjects and methods: The study will involve a total of 1120 patients attending 8 established out-patient clinics in South Asia (140 patients at each clinic). Patients enrolled in the trial will be randomly assigned to either the control (existing care) or the intervention group and will be followed up for an average of 30 months. The total trial duration is about 3.5 years, from mid-August 2010 to December 31, 2013.

NCT ID: NCT01212250 Recruiting - Cirrhosis Clinical Trials

Carvedilol for Pre-primary Prophylaxis of Esophageal Varices in Cirrhosis

Start date: September 1, 2010
Phase: N/A
Study type: Interventional

Patients of cirrhosis aged 18 to 75 years who have no esophageal varices will be enrolled. After baseline evaluation, the participants will be randomized to receive either Placebo or Carvedilol 12.5 mg BD. After randomization they will be followed up for one year.

NCT ID: NCT01209338 Recruiting - Cervical Cancer Clinical Trials

Acceptability and Feasibility of Human Papilloma Virus Vaccine

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

The overall program goal is to determine the Acceptability and Feasibility of introducing a population based Human Papilloma Virus (HPV) Vaccination programme and understanding the key individual and community factors that would determine the potential acceptability of the vaccine.

NCT ID: NCT01206400 Recruiting - Clinical trials for Type 2 Diabetes Mellitus

Effect of Pioglitazone on Testosterone in Eugonadal Men With Type 2 Diabetes Mellitus - A Pilot Study

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

To study the effects of pioglitazone on the steroidogenic enzyme axis in eugonadal men with type 2 diabetes mellitus.

NCT ID: NCT01190579 Recruiting - Clinical trials for Coronary Artery Disease

Dual Source CT Angiography for Detection of Coronary Artery Stenoses

MEDIC
Start date: August 2009
Phase: N/A
Study type: Observational

The trial will investigate the accuracy of Dual Source CT coronary angiography to detect coronary artery stenoses in patients with chest pain who have, based on clinical criteria, an intermediate likelihood for the presence of coronary artery stenoses. No beta blockers will be used to lower the heart rate for the examination. The hypothesis is that Dual Source CT will allow the detection of vessels with at least one coronary artery stenosis with a sensitivity of more than 90%.

NCT ID: NCT01182831 Recruiting - Pancreatic Cancer Clinical Trials

Trial Comparing Two Techniques of Celiac Plexus Neurolysis for Treatment of Pain in Carcinoma Pancreas

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

Coeliac plexus neurolysis (CPN) is a management option for pain control in carcinoma pancreas.CPN is conventionally performed by percutaneous technique with fluoroscopic guidance. Endoscopic ultrasound (EUS) is increasingly used for CPN as it offers a better visualization of the plexus. There are limited data comparing the two modalities.The patients are on follow-up for 6 months post neurolysis.

NCT ID: NCT01178372 Recruiting - Clinical trials for Hepatic Encephalopathy

Secondary Prophylaxis of Hepatic Encephalopathy in Cirrhosis

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

Hepatic encephalopathy (HE), a challenging complication of advanced liver disease, occurs in approximately 30-45% of patients with cirrhosis. The treatment of choice is non-absorbable disaccharides, such as lactulose and lactitol.Probiotics are effective in the treatment of minimal hepatic encephalopathy which precipitates hepatic encephalopathy. The investigators will assess the effects of lactulose and probiotics for the prevention of recurrence of HE (secondary prophylaxis) in patients after the recovery of an episode of overt hepatic encephalopathy.

NCT ID: NCT01175538 Recruiting - Clinical trials for Hepatic Encephalopathy

Primary Prophylaxis of Hepatic Encephalopathy in Patients With Cirrhosis

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

To assess the effects of lactulose for the prevention of first episode of altered sensorium (hepatic encephalopathy, primary prophylaxis) in patients with cirrhosis.