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Constipation clinical trials

View clinical trials related to Constipation.

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NCT ID: NCT02538367 Completed - Clinical trials for Functional Constipation

Phase 1/2a Trial of YH12852 in Healthy Subjects and Patients With Functional Constipation

Start date: August 2015
Phase: Phase 1/Phase 2
Study type: Interventional

A randomized, double-blind/open-label, placebo/active-controlled, single/multiple dose, parallel, phase 1/2a trial to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of YH12852 in healthy subjects and patients with functional constipation

NCT ID: NCT02530216 Completed - Constipation Clinical Trials

Evaluating the Impact of Automated Evaluation of Gastrointestinal Symptoms (AEGIS) on Clinical Outcomes

AEGIS
Start date: April 10, 2017
Phase: N/A
Study type: Interventional

Healthcare delivery now mandates shorter visits with higher documentation requirements, undermining the patient-provider interaction. Electronic health records (EHRs) have the potential to improve outcomes and quality of care in this pressured environment, and are endorsed by the Patient Protection and Affordable Care Act (ACA) and Health Information Technology for Economic and Clinical Health (HITECH) Act as an important mechanism to support value-based healthcare. However, EHR systems were principally designed to support the transactional needs of administrators and billers, less so to nurture the relationship between patients and their providers. The purpose of this research is to identify ways to use EHRs to support clinical gastroenterologists and their patients while meeting the meaningful use requirements of the HITECH Act. To improve clinic visit efficiency and meet criteria for meaningful use, investigators developed a patient-provider portal (P3) that systematically collects patient symptoms using a computer algorithm called Automated Evaluation of Gastrointestinal Symptoms (AEGIS). AEGIS utilizes computerized adaptive testing (CAT) to guide patients through questions drawn from a library of over 300 symptom attributes measuring the timing, severity, frequency, location, quality, and character of their GI symptoms, along with relevant comorbidities, family history, and alarm features. The system then automatically "translates" the patient report into a full narrative HPI available for use by GI providers in an EHR. In a cross-sectional study in the American Journal of Gastroenterology comparing AEGIS versus physician-documented HPIs, investigators found that blinded physician reviewers perceived that AEGIS HPIs were of higher overall quality, better organized, and more succinct, comprehensible, complete and useful compared to HPIs written by physicians during usual care in academic GI clinics. In the current study, investigators aim to evaluate computer-generated HPIs prospectively on a wider scale in diverse academic and community-based settings. Moreover, investigators aim to test an enhanced AEGIS intervention that ties patient HPIs to an individualized "education prescription" which guides the patient through a library of multi-media educational materials on GI symptoms, conditions, and treatments.

NCT ID: NCT02526849 Recruiting - Clinical trials for Slow Transit Constipation

Efficacy and Safety of Fecal Microbiota Transplantation for Slow Transit Constipation

Start date: November 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of fecal microbiota transplantation in adults with slow transit constipation.

NCT ID: NCT02495623 Completed - Clinical trials for Irritable Bowel Syndrome With Constipation (IBS-C)

A Study of the Effect of SYN-010 on Subjects With IBS-C

Start date: June 2015
Phase: Phase 2
Study type: Interventional

A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multi-Dose Study of the Effect of Two Dosage Strengths of SYN-010 Compared with Placebo on Breath Methane Production in Breath Methane-Positive Subjects with Irritable Bowel Syndrome with Constipation (IBS-C)

NCT ID: NCT02493452 Completed - Clinical trials for Irritable Bowel Syndrome Characterized by Constipation

Second Plecanatide Study In Irritable Bowel Syndrome With Constipation (IBS-C)

IBS-C
Start date: June 2015
Phase: Phase 3
Study type: Interventional

This study in patients with IBS-C is a randomized, double-blind, placebo-controlled, parallel-group clinical trial with 12 weeks of study drug therapy.

NCT ID: NCT02493036 Completed - Clinical trials for Irritable Bowel Syndrome With Constipation (IBS-C)

A Single-Dose, Open-Label, Study to Evaluate the Sustainability of the Effects of SYN-010 in Patients With IBS-C

Start date: October 2015
Phase: Phase 2
Study type: Interventional

A Single-Dose, Open-Label, Extension Study to Evaluate the Sustainability of the Effects of SYN-010 in Patients with Irritable Bowel Syndrome with Constipation

NCT ID: NCT02481947 Completed - Clinical trials for Chronic Idiopathic Constipation

A Safety and Efficacy Evaluation of BLI400 Laxative in Constipated Adults

Start date: May 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate a daily dose of BLI400 Laxative for safety and efficacy versus lubiprostone in constipated adults.

NCT ID: NCT02467972 Completed - Diabetes Clinical Trials

Functional Ingredients: Effect in Gastrointestinal System

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

The addition of fructans or unripe banana flour to frozen meals can change the hormonal parameters related to hunger and satiety, improve the bowel movements and increase in colonic bacteria population measured by microbiological determinations (qPCR). The inulin no can change bowel movements and increase in colonic bacteria population measured by microbiological determinations (qPCR)

NCT ID: NCT02461485 Completed - Healthy Clinical Trials

Effect of a Fermented Milk Product With Probiotics Alone or in Combination With Fibers on Constipation Symptoms

Start date: May 2015
Phase: N/A
Study type: Interventional

First experimental study (Proof Of Concept) to investigate bowel function parameters on which a fermented milk product with probiotics alone or in association with fibers has a potential effect.

NCT ID: NCT02459808 Withdrawn - Constipation Clinical Trials

Gastrointestinal Transit Time in Patients With Guillain-Barré Syndrome

Start date: May 2015
Phase: N/A
Study type: Observational

Constipation is a common condition among patients with Guillain-Barré Syndrome. It is believed, that the constipation is caused by autonomic neuropathy. However, the severity of the constipation, and its relation to autonomic function have not previously been studied.