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Constipation clinical trials

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NCT ID: NCT02291679 Completed - Clinical trials for Chronic Idiopathic Constipation

Trial of Linaclotide in Patients With Chronic Idiopathic Constipation

Start date: October 2014
Phase: Phase 3
Study type: Interventional

The objective of this trial is to determine the efficacy and safety of linaclotide administered to patients with chronic idiopathic constipation (CIC). The primary efficacy parameter is the percentage of patients in each dosing group that meet the protocol definition for Complete Spontaneous Bowel Movement (CSBM) Overall Responder.

NCT ID: NCT02291354 Recruiting - Clinical trials for Slow Transit Constipation

Evaluating the Synergism of Soluble Dietary Fiber With Fecal Microbiota Transplantation in Slow Transit Constipation

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

The purpose of this study is to evaluate the synergism of Soluble Dietary Fiber with Fecal Microbiota Transplantation in Adult Patients with Slow Transit Constipation.

NCT ID: NCT02281630 Completed - Clinical trials for Chronic Constipation

Phase II Dose-Finding Study of KWA-0711 in Patients With Chronic Constipation (CC)

Start date: October 15, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of KWA-0711, and to determine its optimal dose in Chronic Constipation (CC) patients.

NCT ID: NCT02270983 Completed - Clinical trials for Opioid-Induced Constipation

Phase 2 Randomized, Double-Blind, Placebo-Controlled, Parallel Group Trial of Linaclotide Administered to Patients With Opioid-Induced Constipation Receiving Chronic Opioid Treatment for Non-Cancer Pain

Start date: October 31, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study was to evaluate the safety and efficacy of linaclotide for the treatment of opioid-induced constipation (OIC), in adults receiving stable opioid treatment for chronic non-cancer pain that has been present for a minimum of 3 months. This study included up to a 4-week Screening Period, and a 2 to 3-week Pretreatment Period. Patients meeting the entry criteria were randomized to 1 of 2 doses of linaclotide or placebo once per day for 8 weeks. This 8-week study assessed the effects of linaclotide on bowel movement frequency, as well as other bowel symptoms of OIC.

NCT ID: NCT02270450 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

S1316, Surgery or Non-Surgical Management in Treating Patients With Intra-Abdominal Cancer and Bowel Obstruction

Start date: March 9, 2015
Phase: N/A
Study type: Interventional

This partially randomized clinical trial studies surgery or non-surgical management in treating patients with intra-abdominal cancer and bowel obstruction. Bowel obstruction is a common problem for advanced cancer patients and can negatively affect quality of life. It is not yet known whether surgery or non-surgical management is the best treatment option for bowel obstruction and can lead to better quality of life.

NCT ID: NCT02255747 Recruiting - Constipation Clinical Trials

Anal Dilatation for Infants and Children With Constipation

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

This study is to evaluate the effect of anal dilation in infants and children with constipation.

NCT ID: NCT02246647 Completed - Clinical trials for Irritable Bowel Syndrome

Biomarkers for Intestinal Permeability in Patients With Constipation

Start date: September 2014
Phase:
Study type: Observational

Our overall objective with this study is firstly to provide a comprehensive assessment of intestinal permeability, mucosal barrier function using existing biomarkers and secondly to explore novel biomarkers for measuring intestinal permeability in patients with constipation predominant Irritable Bowel Syndrome (IBS-C).

NCT ID: NCT02239510 Terminated - Clinical trials for Chronic Idiopathic Constipation

Efficacy of Linaclotide to Senna for CIC

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

In this prospective, randomized, double blind study, the aim is to determine the efficacy of Linaclotide in relation to Senna in relieving the symptoms of chronic idiopathic constipation (CIC). Patients with CIC, (age 18 - 70) will be enrolled in the study and randomized to Senna or Linaclotide. Patients will be asked to complete questionnaires during the study and will be followed for 12 weeks. Main outcomes include number of daily bowel movements and measures from surveys regarding bowel habits, relief, and satisfaction.

NCT ID: NCT02236533 Completed - OBESITY Clinical Trials

Healthy Effects of an Innovative Probiotic Pasta

SFLABPASTA
Start date: March 2014
Phase: N/A
Study type: Interventional

The aim of the project was the evaluation of the antioxidant and anti-inflammatory effects of a whole grain pasta, enriched in barley β-glucans and fortified with strains of Bacillus coagulans, versus a control wheat pasta on healthy volunteers, using a parallel randomized controlled trial.

NCT ID: NCT02234518 Completed - Constipation Clinical Trials

Fibers and Gut Health

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

Gastrointestinal discomfort regularly affects >25% of the population worldwide. One of the major contributors to GI discomfort is constipation, which has a prevalence of ~15% and symptoms of which have a significant negative impact on the sufferer's quality of life. One of the hallmarks of chronic constipation is slow progression of contents through the gut (i.e. slow gut / colonic transit time), which may be associated with hard stools that are difficult to expel. Dietary fiber supplements are widely used as a first-line treatment for constipation although little Level 1 evidence exists to support its use in adults. The effectiveness of different fiber supplements is difficult to compare given wide differences in water-retention capabilities and effects on the colonic microbial ecology. Given the promising, yet largely unsubstantiated, benefits of fiber supplementation on symptoms of functional constipation, the objective of this clinical trial is to evaluate tolerance and effectiveness of four week supplementation of a fiber product, in a dose-ranging fashion, on whole gut transit time and gastrointestinal symptoms in adults with functional constipation.