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Tolerance clinical trials

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NCT ID: NCT02307773 Completed - Tolerance Clinical Trials

Lidocaine Spray on an Endoscope to Improve Tolerance to Endoscopy

Start date: November 2013
Phase: N/A
Study type: Observational

The investigators tested whether a new method which additional lidocaine spray on the tip of endoscope can increase the tolerance of examinee during endoscopy than conventional pharyngeal anesthesia alone.

NCT ID: NCT02144402 Completed - Infant Development Clinical Trials

Growth of Healthy Term Infants Fed Formula Containing DHA-B

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

The primary objective is to determine if the weight gain of healthy term infants fed a commercially available term infant formula supplemented with DHASCO® is similar to that of infants fed the same formula supplemented with a new product, DHASCO®-B.

NCT ID: NCT02091349 Completed - Tolerance Clinical Trials

Tolerance and Utilization of Polydextrose, Inulin, and Soluble Corn Fiber

Start date: July 2010
Phase: N/A
Study type: Interventional

The objective of this study is to determine the tolerance and utilization of polydextrose and soluble corn fiber through analyses of fecal samples of fermentative end-products (short-chain fatty acids, ammonia, phenol, and indole) and shifts in microbial populations.

NCT ID: NCT02016703 Completed - Tolerance Clinical Trials

Gastrointestinal Tolerance of Erythritol-containing Beverages in Young Children

Start date: March 2006
Phase: N/A
Study type: Interventional

Purpose of this study: assess the maximum tolerated bolus dose of erythritol, delivered in a clear beverage, compared with placebo (saccharose) in 4-6 year old children.

NCT ID: NCT01925560 Completed - Tolerance Clinical Trials

Tolerance and Utilization of Agave Inulin in Healthy Adults

Start date: January 2013
Phase: N/A
Study type: Interventional

The objective of this study is to assess the tolerance and utilization of agave inulin. This will be accomplished through analyses of breath and fecal samples to quantify fermentation end-products- hydrogen, carbon dioxide, and methane will be measured in the breath, and short-chain fatty acids, ammonia, phenol, and indole will be measured in feces. Microbial populations will also be measured in fecal samples.

NCT ID: NCT01909661 Completed - Tolerance Clinical Trials

Tolerance of Infants With Cow's Milk Protein Allergy to Extensively Hydrolyzed Rice Protein or Casein Infant Formulas

JUNGLO
Start date: March 2013
Phase: Phase 2
Study type: Interventional

The objective of this double blinded randomized study is to assess the tolerance of two extensively protein hydrolyzed infant formulas, one based on rice protein and the other one on casein, at introduction, and after 3 months of consumption, and their efficacy on growth and on the reduction of allergy symptoms through a 3 months consumption period.

NCT ID: NCT01873820 Completed - Tolerance Clinical Trials

Tolerance of Two Forms of Vitamin C in Acid-sensitive Adults

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the tolerance of two forms of vitamin C in adults with sensitivity to acidic foods.

NCT ID: NCT01346644 Completed - Tolerance Clinical Trials

Safety of Lactobacillus Fermentum in Newborn Infants

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

In the last years manipulation of intestinal microbiota with probiotics has gained an increasing interest, specially in infant nutrition since recent studies has demonstrated the presence of probiotics in human milk. However, there are few studies studying the effects of probiotics in newborns. The objective of the present study is to analyze safety and tolerance of the probiotic Lactobacillus fermentum CECT5716 isolated from human milk.

NCT ID: NCT01038882 Completed - Anxiety Clinical Trials

Randomized Study With Midazolam for Sedation in Flexible Bronchoscopy

Start date: October 2008
Phase: N/A
Study type: Interventional

The Flexible Bronchoscopy (FB) is a diagnostic and therapeutic procedure which is not usually tolerated by the patient. This makes the examination more difficult and a repetition of the examination, if necessary, resulting in a lower diagnostic performance. Furthermore, there is nowadays little information with a highly obvious level about the relationship between sedation and the patient´s satisfaction with the FB. Midazolam is one of the most commonly used sedatives at the beginning for its rapid onset property and brief duration of action with sedatives, anxiolytics and amnesia properties. The principal aim of our study is to analyse if the use of a local anaesthetic with midazolam whilst performing an FB improves the quality of examination in terms of tolerance for the patient. It would also be of interest to know if there is an improvement in the acceptance of a second or further FB and if this improves the satisfaction of the Bronchoscopist as far as the examination performed is concerned.