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NCT ID: NCT01685736 Recruiting - Hypertension Clinical Trials

Ambulatory Versus Home Blood Pressure Monitoring in Obstructive Sleep Apnea

OSA
Start date: February 2012
Phase: N/A
Study type: Observational

Subjects referred to a sleep clinic had polysomnography (PSG), clinic BP measurements, 24-hour ABP monitoring and HBP monitoring using a device (Microlife WatchBP HomeN) that allows daytime (3 days, 2 duplicate readings/day) and automated nighttime BP measurement (3 nights, 3 readings/night).

NCT ID: NCT01675505 Recruiting - Clinical trials for Adaptation, Psychological

Psychological Well-being Outcomes in Disease-free Survivors of Colorectal Cancer Following Curative Surgery

Start date: May 2012
Phase: N/A
Study type: Observational

The purpose of the study is to investigate whether there are prognostic factors regarding the mental and functional adjustment of colon cancer patients following curative surgery. Patients will be selected using specific inclusion criteria. Prognostic factors investigated include personality characteristics, initial distress, medical, social and economic factors. The utmost purpose of the study is to assist clinicians with the timely identification of vulnerable patients in order to ensure their proper management and their optimal adjustment. Moreover this is the first study using the Distress Thermometer in Greek patients with cancer.

NCT ID: NCT01633489 Recruiting - Clinical trials for Lysosomal Acid Lipase Deficiency

Lysosomal Acid Lipase (LAL) Deficiency Registry

ALX-LALD-501
Start date: December 31, 2012
Phase:
Study type: Observational [Patient Registry]

This is an observational, multi-center, international disease registry designed to collect longitudinal data and create a knowledge base that will be utilized to improve the care and treatment of patients with LAL Deficiency. Participation in the Registry by both physicians and patients is voluntary.

NCT ID: NCT01629394 Recruiting - Morbid Obesity Clinical Trials

Comparative Study of Sugammadex Versus Neostigmine for Reversal of Neuromuscular Blockade in Morbidly Obese Patients

Start date: January 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Postoperative residual curarization in the post anaesthesia unit has been associated to complications involving respiratory function and impaired laryngeal and pharyngeal muscles' function. Speed of reversal of neuromuscular blockade after administration of sugammadex versus neostigmine has been studied, but up to date no data are available concerning continuous acceleromyography monitoring of adductor pollicis and corrugator supercilii in morbidly obese patients undergoing weight loss surgery. The investigators' aim in this prospective, double-blinded study was to compare train of four ( TOF ) values, the presence or absence of clinical criteria of postoperative residual curarization , the dose requirements and the side effects of sugammadex and neostigmine for the reversal of rocuronium induced neuromuscular blockade in patients undergoing laparoscopic or open surgery for morbid obesity.

NCT ID: NCT01607242 Recruiting - Thyroidectomy Clinical Trials

Impact of Total Thyroidectomy on Voice and Swallowing

Start date: March 2012
Phase: N/A
Study type: Observational

Purpose of this study is to evaluate the outcome of total thyroidectomy on vocal and swallowing function.

NCT ID: NCT01582607 Recruiting - Clinical trials for Stillborn Caesarean Section

Subarachnoid Administration of Levobupivacaine for Cesarean Section

Start date: January 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the investigators study is to compare the clinical effects and side-effects of these three local anaesthetics as sole agents or with the supplementation with fentanyl for c-section, especially when administered in doses achieving approximately an ED 50.

NCT ID: NCT01558713 Recruiting - Clinical trials for Stillborn Caesarean Section

Epidural Volume Extension and Intrathecal Use of Local Anesthetics in Cesarean Sections

Start date: January 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Intrathecal (i.t.) administration of isobaric bupivacaine, ropivacaine and levobupivacaine with addition of fentanyl for c-section either combined or not with administration of 10 ml of N/S 0,9% epidurally, in order to extent epidural space.Sensory and motor block profile, haemodynamics and side effects were assessed.

NCT ID: NCT01546077 Recruiting - Foot Surgery Clinical Trials

Placement of Perineural Catheters in the Popliteal Region

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy of the hydrolocalization technique for placement of popliteal perineural catheters in comparison with the stimulating catheters. A non inferiority trial.

NCT ID: NCT01533584 Recruiting - Clinical trials for Nocturnal Hypertension

Evaluation of Nocturnal Hypertension and Correlation With Target-Organ Damage

Start date: March 2012
Phase: N/A
Study type: Observational

The aim of this study is to evaluate nocturnal hypertension with 24-hour ambulatory blood pressure and home blood pressure (BP) measurements through a) comparison of mean BP and nocturnal dipping assessed with the two methods, b) correlation of those parameters with parameters of target-organ damage and c) comparison of the potential of the two methods to define non-dippers.

NCT ID: NCT01524276 Recruiting - Clinical trials for Coronary Artery Disease

Product Surveillance Registry

PSR
Start date: January 2012
Phase:
Study type: Observational

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.