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NCT ID: NCT01511237 Completed - HIV Infections Clinical Trials

Perinatal Antiretroviral Intensification for PMTCT of HIV in Late Comers

PHPT-5
Start date: December 2011
Phase: Phase 3
Study type: Interventional

The purpose is to evaluate the efficacy of maternal and infant perinatal antiretroviral prophylaxis intensification for the prevention of mother-to-child intrapartum transmission of HIV-1 in women receiving less than 8 weeks of antiretroviral prophylaxis during pregnancy.

NCT ID: NCT01509118 Recruiting - Clinical trials for Open Fracture of Hip

Rivaroxaban Safety Profile in the Prophylaxis of Venous Thromboembolism After Hip Fracture Surgery

Start date: July 2011
Phase: N/A
Study type: Observational

Arterial and venous thromboembolism represents one of the most common preventable health problems. Patients undergoing surgery, especially hip fracture surgery are at high risk for deep vein thromboembolism (VTE) without thromboprophylaxis. In the absence of prophylaxis, the incidence of fatal pulmonary embolism (PE) after Hip Fracture Surgery (HFS) is reportedly 4%-12%. Provision of thromboprophylaxis to all patients who undergo HFS is recommended.

NCT ID: NCT01507935 Withdrawn - Healthy Infants Clinical Trials

Colonisation Resistance Study

ColoR
Start date: January 2012
Phase: Phase 2
Study type: Interventional

This study is initiated to investigate the effect of infant formulas with added specific prebiotic oligosaccharides on the reduction of specific potential pathogens and/or toxins.

NCT ID: NCT01505920 Completed - Clinical trials for Uterine Cervical Dysplasia

Lidocaine Spray Compared With Submucosal Injection During LEEP: a Randomized Controlled Trial

Start date: September 2011
Phase: Phase 3
Study type: Interventional

Loop Electrosurgical Excision Procedure (LEEP) is a widely used minor surgical procedure for diagnosis and treatment of cervical intraepithelial neoplasia. During the procedure, several methods have been proposed to reducing pain including submucosal block, paracervical block, and oral analgesics. Submucosal (underneath the lining of the cervix) injection of lidocaine appeared to be the most common methods used. However, from the investigators experience, there is significant pain associated with the injection itself. Lidocaine spray is an effective measure for pain control during minor gastrointestinal and otolaryngological procedures. It is simple without pain related to application. An objective of this study is to examine effectiveness of lidocaine spray versus lidocaine submucosal injection by comparing pain scores at various stages of the LEEP procedure.

NCT ID: NCT01502540 Completed - Pain Clinical Trials

Pain Prevalence After Major Craniotomy

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

Craniotomies are generally thought to be less painful than other operations. Indeed recent studies have confirmed that pain is a common problem during the postoperative phase following craniotomy.Pain not only causes discomfort, but it is also associated with other potential adverse events such as increased sympathetic activity and elevated systemic blood pressure. These events in turn may contribute to increased intracranial pressure. Some patients may also develop chronic pain.Potent opioids have been avoided due to its potential to cause respiratory depression and risk of masking pupillary signs. As a result postoperative craniotomy pain controls are usually inadequate. In Siriraj hospital, there are 500-600 craniotomy patients per year. Still there are no definite guidelines for postoperative pain management in these patents due to lack of information about quality of postoperative pain control after craniotomy. Objectives Primary objective : - To study incidence of moderate to severe pain during first 48 hours after craniotomy. Secondary objectives : - To determine risk factors for moderate to severe pain during first 48 hours after craniotomy - To evaluate side effects and complications of postoperative craniotomy pain control - To compare patient's expectation for pain management before and after surgery - To determine patient's satisfaction for postoperative pain management

NCT ID: NCT01501968 Not yet recruiting - Drug Safety Clinical Trials

Efficacy of Ascorbic Acid for Prevention of Colistin-Associated Nephrotoxicity

Start date: January 2012
Phase: Phase 3
Study type: Interventional

Ascorbic acid (Vitamin C) could protect renal toxicity from colistin.

NCT ID: NCT01501474 Terminated - Clinical trials for Malignant Biliary Strictures

Utility of CholangioFlex and Fluorescent in Situ Hybridization in the Diagnosis of Malignant Biliary Strictures

Start date: January 2012
Phase:
Study type: Observational

Utility of CholangioFlex and Fluorescent in situ Hybridization in the Diagnosis of Malignant Biliary Strictures Objectives 1. To assess the sensitivity, specificity and accuracy of CholangioFlex in malignant biliary stricture diagnosis 2. To assess the sensitivity, specificity and accuracy of Fluorescent in situ Hybridization(FISH) in malignant biliary stricture diagnosis Study design One academic center, prospective, diagnostic study Research Methodology Target population: Patients who are diagnosed malignant biliary stricture. Sample population: Patients who are diagnosed malignant biliary stricture in Chulalongkorn Hospital

NCT ID: NCT01501422 Completed - Clinical trials for Insomniac Postmenopausal Women

Effect of Estrogen Therapy on Objective Sleep Quality in Postmenopausal Women

Start date: July 2011
Phase: Phase 3
Study type: Interventional

1. Sex hormone including estrogen have synergistic effect to serotonin activity and decrease activity of monoamine oxidase activity so the norepinephrine is not be metabolized, these substance are important to regulate hemostasis and circadian process of sleep 2. Estrogen also regulate gamma-aminobutyric acid (GABA) secretion - GABA substance is in order to initiate sleep and continue sleep 3. According to epidemiologic data, problem of sleep was increasing in postmenopause group compare to premenopause group (aged-match) 4. This research perform to find out the actual effect of estrogen in improving sleep quality.

NCT ID: NCT01500291 Enrolling by invitation - Depression Clinical Trials

A Study Survey of Stress in Anesthesia Personnel

stress
Start date: April 2012
Phase: N/A
Study type: Observational

It is inevitable that nearly both anesthesiologist and nurse anesthetist take a zero tolerance approach to avoidable safety problems in the provision of anesthesia. We would like to study the stress upon anesthesia personnel by using Suanprung Stress Test (SST) - a well-documented, psychological stress test, and Siriraj Anesthesia-related Stress Test (SAST) - a new developed open-ended opinion poll, to scrutinize the daily rounds stress and yield the solution to eradicate or alleviate those worries as well as improve both physical and mental health to handle the situation of difficulties.

NCT ID: NCT01500239 Completed - Clinical trials for Complicated Intra-Abdominal Infection

A Study Comparing Ceftazidime-Avibactam+Metronidazole Versus Meropenem in Adults With Complicated Intra-abdominal Infections

Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effects of Ceftazidime Avibactam plus Metronidazole compared to Meropenem for treating hospitalized patients with complicated intra-abdominal infections.