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Constipation clinical trials

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NCT ID: NCT04671030 Completed - Clinical trials for Spinal Cord Injuries

Use of a Prokinetic Agent as an Adjunct to Thrice Weekly Bowel Care After SCI

TWBC
Start date: January 15, 2018
Phase: Phase 1
Study type: Interventional

To measure a baseline for each subject, an abdominal x-ray (KUB) was performed, the SCI Bowel Survey and Treatment Satisfaction Questionnaire (TSQM) were administered and the subject's weight determined. After all the baseline measurements were acquired, the subjects underwent transdermal screening with hair epilation to test their response to transdermal administration of NEO (0.07mg/kg) and GLY (0.014mg/kg). All subjects had a positive response (bowel movement within 60 minutes of drug administration) and received five more cycles of bowel care for two weeks. All subjects reported bowel evacuation during each session and some reported side effects like slight dry mouth, eye twitching, and cramping. These side effects lasted approximately 20-30 minutes in duration and there were no clinically significant changes in cardiopulmonary vital signs. Six subjects after completing two weeks of bowel care had an abdominal x-ray (KUB) done. Also, they were weighted and reassessed using the TSQM and bowel survey.

NCT ID: NCT04667884 Completed - Constipation Clinical Trials

Effects of Prebiotic or Probiotic Supplements on Symptoms of Functional Constipation

Start date: August 15, 2020
Phase: N/A
Study type: Interventional

This study intends to evaluate the effects of three prebiotic solid beverages (mainly dietary fiber and prebiotics) and one probiotic solid beverage on the laxative effect of patients with functional constipation through randomized controlled trials. The influence of tract flora is expected to provide a basis for related therapies for patients with functional constipation.

NCT ID: NCT04647045 Completed - Clinical trials for Irritable Bowel Syndrome With Constipation

An Evaluation of Cultured Milk Drink on Immune Status of Patients With Irritable Bowel Syndrome: Constipation Predominant

Start date: May 2, 2017
Phase: N/A
Study type: Interventional

Our previous work on the use of probiotics improved the clinical symptoms in irritable bowel syndrome with constipation-predominant. This study would like to explore further use of probiotics in the immune system of the patients with irritable bowel syndrome.

NCT ID: NCT04627610 Completed - Rectal Prolapse Clinical Trials

Recurrence of Dyschezia in Rectal Prolapse, Rectocele and Elytrocele

PEXITY
Start date: March 9, 2022
Phase:
Study type: Observational

Prolapse of the rectum is a pathology that preferentially affects older women with a significant impact on quality of life. A very large number of therapeutic approaches can be proposed (functional treatment, surgical techniques by perineal approach and surgical techniques by anterior approach). D'Hoore and Pennix described Ventral Rectopexy with prosthetic reinforcement which is accepted as a standard of treatment in much of Europe for externalized prolapse but remains maligned in much of the world. Due to the relatively recent appearance of this technique and the great variability in the management methods, the long-term results of Ventral Rectopexy have been little studied. This surgical technique is the preferred approach offered at CHU Grenoble Alpes. Pr Faucheron have internationally recognized experience in surgical grip with a very high patient volume in recent years.

NCT ID: NCT04620317 Completed - Clinical trials for Functional Constipation

Effects of Synbiotics on FC and Other Contributing Factors

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

Prevalence of functional constipation (FC) was first determined with 15.2% reported. Next, a 16-week randomised, double-blind, placebo-controlled study conducted to assess the improvement in functional constipation among the respective individuals by using synbiotic supplement. Throughout the intervention, it was reported that significant improvements for defecation frequency, Bristol Stool Form (BSF) scale, and Patients Assessment of Constipation Symptoms (PAC-SYM) scores were reported within synbiotic group (p < 0.001). However, no significant different was reported when compared both groups as placebo group was found to have significant within-group difference too. Placebo effect was suspected in this study.

NCT ID: NCT04620161 Completed - Clinical trials for Functional Constipation

A Proof of Concept Study of Pradigastat in Patients With Functional Constipation

Start date: September 22, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy, safety, and tolerability of pradigastat 20 and 40 mg as compared to placebo in patients with Functional Constipation.

NCT ID: NCT04614935 Completed - Pediatric ALL Clinical Trials

Adherence and Outcomes in Functional Constipation With a Constipation Action Plan

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

We will be assessing for improvement in reported symptoms as well as reported quality of life in pediatric patients with functional constipation using a constipation action plan and an adherence log.

NCT ID: NCT04590846 Completed - Constipation Clinical Trials

A Caregiver-mediated Health Educational Intervention to Improve Constipation Status of Primary School Children

Start date: October 7, 2020
Phase: N/A
Study type: Interventional

The research adopts caregiver-mediated health educational intervention to Improve constipation status of primary school children. It is a quasi-experimental design study, which will enroll students in the 3rd to 6th grades of two primary schools and their parents in Yunlin County. There will be 200 children in the experimental group and 200 in the control group. Parents in the experimental group will receive health educational leaflets every week and no intervention will be given to the control group. Both the experimental and control groups students will be asked to fill up a questionnaire at the before and after the intervention with a total of 8 weeks. The study can provide the understanding of the current status of constipation in primary school children, parents' awareness and attitudes on constipation-related issues.

NCT ID: NCT04587635 Completed - Clinical trials for Constipation - Functional

Evaluation of Changes in Bowel Movement Frequency Following the Consumption of PHGG in Adults With Constipation

TYPHOON
Start date: September 16, 2020
Phase: N/A
Study type: Interventional

Evaluation of Changes in Bowel Movement Frequency Following the Consumption of Partially Hydrolyzed Guar Gum (PHGG) in Adults with Constipation

NCT ID: NCT04569656 Completed - Parkinson Disease Clinical Trials

Treatment of Chronic Constipation in Parkinson's Disease

PHGG-PD
Start date: February 2, 2016
Phase: Phase 2
Study type: Interventional

Chronic constipation is the most common gastrointestinal symptom reported by PD patients; it could be one of the manifestations of disease onset. PHGG fiber is extracted from a herbaceous plant (Cyamopsis Tetra-Gonolobus, family: Leguminosae) of Indian origin: it produces 5/9 pods containing seeds which produce the famous guar gum, that is a natural polysaccharide.