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Constipation clinical trials

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NCT ID: NCT02122471 Completed - Clinical trials for Chronic Idiopathic Constipation

12-Week Study of Plecanatide for CIC (The National CIC3 Study)

CIC
Start date: April 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to confirm that the investigational medication, plecanatide, is safe and effective in treating chronic idiopathic constipation.

NCT ID: NCT02116101 Completed - Constipation Clinical Trials

Intestinal Health and Blood Lipid Adjustment

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

This was a randomized, double-blind, single-center, placebo-controlled, two-arm study. The objectives of this study were to evaluate the effect of Momchilovtsi yogurt on: 1. Improving intestinal digestion and bowl movement; 2. Adjusting blood total Cholesterol and Triglycerides levels; 3. Adjusting microbiological flora (Clostridium perfringens bacteria, Lactobacillus and Bifidobacterium) in gastrointestinal tract; 4. Adjusting short chain fatty acids (acetic acid, propionic acid, butyric acid) in in gastrointestinal tract.

NCT ID: NCT02110719 Completed - Pain Clinical Trials

Decreasing Narcotics in Advanced Pelvic Surgery

Pain
Start date: March 2014
Phase: Phase 4
Study type: Interventional

In recent years, there has been an emphasis on the creation of "enhanced-recovery", "fast-track" or "multi-modal" pathways to improve perioperative care (1-4). The goal of these programs is to reduce the length of hospital stay, decrease narcotic usage while improving pain control, accelerate post-operative recovery, and expedite return to baseline functional status. Pathways often are developed by a team of surgeons, nurses, pain specialists, anesthesiologists and other support staff. Postoperative components often involve multi-modal analgesia, early return to activity and early return to a regular diet. The goal of this study is to evaluate the efficacy of a multi-modal pain regimen in advanced pelvic surgery with a primary goal of decreasing narcotic usage.

NCT ID: NCT02103556 Completed - Clinical trials for Chronic Kidney Disease

Edible Oils in the Treatment of Constipation of Hemodialysis Patients

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

The purpose of this study was to evaluate the effect of olive oil and flaxseed oil in the treatment of constipation of patients undergoing hemodialysis.

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: NCT02091115 Completed - Constipation Clinical Trials

Consumption of Milk Drink and Constipation

Start date: July 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Constipation is a disorder which can be associated with various pathologies or could also be an effect of the consumption of drugs, improper diet and life style. Is increasingly common the utilization of probiotics in foods. Probiotics are defined as live microorganisms administered in adequate amounts confer a health benefit to the host, the most widely used for milk-based drinks are lactic bacteria Lactobacillus and Bifidobacterium. The objective of the present study is to assess the effectiveness of the consumption of dairy beverage enriched with probiotic for the treatment of the symptoms of constipation.

NCT ID: NCT02082457 Completed - Clinical trials for Irritable Bowel Syndrome

Efficacy and Safety of YKP10811 in Subjects With Irritable Bowel Syndrome With Constipation

YKP
Start date: December 2013
Phase: Phase 2
Study type: Interventional

This trial is to investigate efficacy and safety of YKP10811 in Subjects With Irritable Bowel Syndrome With Constipation. The difference of responder rate between test group (10, 20 and 40mg) and placebo will be evaluated.

NCT ID: NCT02078323 Completed - Clinical trials for Irritable Bowel Syndrome With Constipation (IBS-C)

Investigation of Linaclotide's Effect on the Bi-directional Brain and Gut Axis in IBS-C Patients

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

The purpose of this study is to understand how a drug called Linaclotide improves bowel function and abdominal pain in patients with Irritable Bowel Syndrome with Constipation (IBS-C) as well as to examine whether Linaclotide alters communication between the brain and pelvic-floor region. Linaclotide has been shown to improve abdominal pain and bowel symptoms in IBS-C, and is approved by the FDA for the treatment of this condition. However, how exactly this drug works to relieve abdominal pain and discomfort in humans is not clearly known. Studies in animal models suggest that patients with IBS-C have hypersensitivity in the gut. Consequently, in IBS-C patients, there is rapid and excessive conduction of signals both from the brain and central nervous system region towards the pelvic-floor (anorectal axis) and the reverse direction. The investigators hypothesize that treatment with Linaclotide may improve/normalize these signals and thereby improve bowel symptoms. Investigators will test this theory using a new, noninvasive (and established) method of studying this communication pathway between the brain and gut.

NCT ID: NCT02073006 Completed - Constipation Clinical Trials

A Study to Evaluate the Effects of a Natural Supplement in Adults With Chronic Functional Constipation

Start date: February 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Constipation is common in the general population, especially in women and in the elderly. Hard stool is a complaint often associated with constipation, which suggests that stool softening would provide a major benefit in the strategy of treatment. This investigative fibre product is primarily a soluble dietary fibre with added probiotics and a prebiotic. It is not digested in the small intestine and partly remains undigested by bacteria in the gut. Also, as probiotics are believed to help restore a healthy gut flora, reduce pH, assist with digestion of food and reduce gaseous by-products they may aid the improvement of intestinal motility. The objective of this study is to assess if this investigative, fibre product effects the number of bowel movements per week and if this in turn impacts quality of life and symptoms of constipation.

NCT ID: NCT02067546 Not yet recruiting - Constipation Clinical Trials

Innovative Toilet Seat Test for Patients With Symptoms of Constipation and/or Emptying Disorders

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

Emptying disorders are of the most common causes of constipation. An adjustable toilet seat was designed by " Shva-Nach" Ltd company, and is designed to facilitate the angle sitting position. Its efficacy will be evaluated in the current study, on 50 volunteers who suffer from constipation and meet the Rome 3 criteria for constipation.