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Signs and Symptoms, Digestive clinical trials

View clinical trials related to Signs and Symptoms, Digestive.

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NCT ID: NCT02253628 Completed - Stress Clinical Trials

The Acute Effect of Coffee Consumption on Stomach, Self-reported Gastrointestinal Symptoms and Stress.

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

This study investigated the acute effect of the consumption of four different kinds of coffee (hot and cold instant coffee, cold espresso and hot filter coffee) with the same caffeine content on salivary gastrin, cortisol and alpha-amylase concentrations, on self-reported gastrointestinal symptoms and on psychometric assessments in healthy individuals.

NCT ID: NCT02180035 Completed - HIV Clinical Trials

Treatment With Nutritional Eating Plan and Dietary Fibers in Adult Patients With HIV/AIDS

PRECOR-NUT
Start date: October 2009
Phase: N/A
Study type: Interventional

To evaluate if nutritional treatment with nutritional supplementation of dietary fiber reduces cholesterol levels and triglycerides (dyslipidemia) in patients with HIV/AIDS receiving antiretroviral therapy (HAART).

NCT ID: NCT02099591 Completed - Clinical trials for Constipation, Signs and Symptoms, Digestive

Phase I Pharmacokinetics and Safety Study of Naloxegol in Paediatric OIC Patients

Start date: November 2014
Phase: Phase 1
Study type: Interventional

To characterize the pharmacokinetics (PK) of naloxegol after single oral dose and through population PK in paediatric patients with opioid induced constipation (OIC) or at risk of OIC.

NCT ID: NCT02054455 Completed - Clinical trials for Gastrointestinal Symptoms

Proton Pump Inhibitors and Gastrointestinal Symptoms

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

The aim of the study is to evaluate the potential protective effect of Lactobacillus paracasei subspecies paracasei F19 administration on bowel symptom onset in patients with gastro-esophageal reflux disease at long-term PPI treatment.

NCT ID: NCT01927900 Completed - Gut Microbiota Clinical Trials

The Effects Of HMO On The Faecal Microbiota And On Gastrointestinal Symptoms In Healthy Volunteers

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

The study is a randomised, placebo-controlled, double-blind, parallel, dose-finding study with healthy volunteers. A total of 100 male and female volunteers will be included. The volunteers will be randomized into one of 10 groups, each of 10 participants, consuming either active product in various mixes and doses (9 groups) or placebo product (1 group) for 2 weeks. The 9 groups receiving active product will receive either one of two Human Milk Oligosaccharides (HMOs) alone or in combination at different doses. The primary purpose of the study is establishing the effects of various compositions and doses of HMOs on the faecal flora and on gastrointestinal symptoms in health adults.

NCT ID: NCT01684319 Completed - Clinical trials for Gastrointestinal Symptoms in Young Infants

Milk-induced Gastrointestinal Symptoms in Infants

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

Various digestive manifestations are common in infants less than 6 months and have a significant impact on morbidity and quality of life of the family. In a prospective study on more than 2800 Italian infants followed by 0-6 months of life, it was determined that 55% of these children had gastrointestinal symptoms such as regurgitation (23%), colics (20%), constipation (17%) or poor weight gain (15%). However, these symptoms are not very accurate, and their cause is often difficult to determine. Frequently, the pediatrician will exclude cow's milk protein in infant feeding, but without a clear etiological diagnosis was asked. This measure causes significant additional costs through the use of extensively hydrolyzed milk specifically for children and involves an elimination diet of all foods containing cow's milk sometimes for several years. This can negatively influence the growth of the child. If the involvement of milk in these pathologies is suggested by some early studies (35% for colics, 68% in constipation, 42% in gastroesophageal reflux), it is unclear in the current state of knowledge if these gastrointestinal symptoms are actually due to an "allergy" to milk. Moreover, there is no validated diagnostic test for non-IgE-mediated gut allergy. However, various tests have proven their effectiveness in the investigation of non IgE-mediated allergy (eg. LAT, patch tests) and will be used in this study.

NCT ID: NCT01675960 Terminated - Chronic Pain Clinical Trials

Effectiveness of Gabapentin on Chronic Irritability in Neurologically Impaired Children

Start date: April 2012
Phase: Phase 2
Study type: Interventional

This study is a prospective, randomized, double blind, placebo controlled, crossover clinical trial looking at whether gabapentin can provide symptom relief for chronic irritability in neurologically impaired children. The investigators hypothesize gabapentin ins beneficial and safe for children with chronic irritability that persists despite identification and appropriate management of symptom sources.

NCT ID: NCT01623154 Completed - Clinical trials for Bacterial Infection Due to Helicobacter Pylori (H. Pylori)

POCone-UBiT-IR300 Pediatric Comparison Study

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

The purpose of this study is to compare between the POCone® to the UBiT®-IR300 in measuring 13CO2/12CO2 ratio in breath samples when used together with the BreathTek® UBT (urea breath test) Kit and the pUHR-CA web-based software program in identifying H. pylori infection in pediatric subjects.

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: NCT01444859 Active, not recruiting - Clinical trials for Recurrent Gastrointestinal Symptoms

Trenev Trio®/Healthy Trinity® for Recurrent Gastrointestinal Symptoms

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

Clinical trial to compare safety and effectiveness of 10-week supplementation with Trenev Trio®/Healthy Trinity® vs. placebo in otherwise healthy subjects with recurrent gastrointestinal symptoms.