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Signs and Symptoms clinical trials

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NCT ID: NCT01708668 Recruiting - Pain Clinical Trials

The Effects of Intermittent Epidural Bolus on Fever During Labor Analgesia

EIEBFLA
Start date: October 2012
Phase: N/A
Study type: Interventional

Epidural analgesia is associated with maternal intra-partum fever during labor. Intermittent epidural injections appear to reduce the incidence of maternal intra-partum fever compared to continuous epidural infusion during labor analgesia. However, the optimal combination of bolus volume and administrating interval has not yet been compared. The purpose of this prospective, randomized, double-blind trial was to determine how intermittent epidural bolus reduced the incidence of maternal intra-partum fever compared with continuous epidural infusion during labor.

NCT ID: NCT01551238 Recruiting - Obesity Clinical Trials

Energy Expenditure, Sleep and Macronutrients

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

The purpose of this study is to determine energy expenditure and sleep in response to protein/carbohydrate and fat ratio of the diet over a short-term and long-term period of time.

NCT ID: NCT01464814 Recruiting - Clinical trials for Signs and Symptoms, Digestive

Clinical Trial Evaluating the Viability of L. Casei + Fish Oil Capsules

Probiomega
Start date: October 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effects of the probiotic KE-99 Lactobacillus casei when administered with omega-3 fish oil on probiotic viability, fecal make-up and gastrointestinal (GI) health in healthy adults.

NCT ID: NCT01382810 Recruiting - Dry Eye Syndromes Clinical Trials

Altaire Gel Forming Solution Versus Refresh Tears for the Treatment of Dry Eye Signs and Symptoms

Start date: March 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate and compare the effects of Altaire Gel forming solution and Refresh Tears in mild-moderate dry eye patients.

NCT ID: NCT00328029 Recruiting - Clinical trials for Signs and Symptoms, Respiratory

Respiratory Side Effects of Busulfan High Dose Chemotherapy in a Pediatric Population

Start date: July 2006
Phase: Phase 2
Study type: Interventional

Recently, several conditioning regimens did not include total body irradiation (TBI) anymore, especially in the case of young children due to cognitive sequelae and late effects on growth and height. Thus, such effective chemotherapy conditioning regimens were developed to avoid these complications. Busulfan is one of the major drugs used in these treatments, but, is also administered in high dose chemotherapy followed by autograft. In both situations, long term pulmonary side effects were diagnosed in a few cases. Even if the occurrence is not very frequent, the clinical management is a real challenge regarding the reduced quality of life and life expectancy of these patients. Up to now, no correlation was done between respiratory sequelae and busulfan pharmacokinetics. Hence, in the investigators' pediatric onco-hematological unit, a prospective study will begin and last three years to assess the respiratory side effects due to busulfan and their potential links with individual drug pharmacokinetic measures. These results will be compared to patients treated with TBI during the same period of time.

NCT ID: NCT00173706 Recruiting - Anemia Clinical Trials

Evaluation of the Effects of L-Carnitine Injection in Patients Undergoing Hemodialysis

Start date: October 2004
Phase: Phase 4
Study type: Interventional

This is a study designed to test the hypothesis that treatment with L-carnitine will improve the quality of life and some specific symptoms and signs in patients with renal failure submitted to hemodialysis.