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Constipation clinical trials

View clinical trials related to Constipation.

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NCT ID: NCT01781104 Completed - Constipation Clinical Trials

Phase 2 Study to Evaluate Safety and Efficacy of RM-131 Administered to Patients With Chronic Constipation

Start date: March 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate safety and tolerability as well as the effects of RM-131 on colonic transit, bowel consistency, bowel habits, abdominal pain, and other abdominal symptoms in patients with chronic constipation.

NCT ID: NCT01773096 Completed - Constipation Clinical Trials

Methylnaltrexone Use for Opioid-induced Postoperative Constipation

Start date: May 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the routine use of methylnaltrexone in the post-operative pediatric spinal fusion patient will decrease the incidence of constipation.

NCT ID: NCT01734226 Recruiting - Constipation Clinical Trials

Efficacy and Safety of Prunus Mume Extract on Improvement of Constipation

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

The investigators performed a 8-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Prunus Mume Extract on Improvement of Constipation. The investigators measured Improvement of Constipation parameters , including Colonic Transit Time, number of bowel movement, defecation time, stool type, color and stool amounts per defecation, and monitored their blood pressure.

NCT ID: NCT01726751 Completed - Pain Clinical Trials

Spinal Cord Stimulation for Pain Relief in Irritable Bowel Syndrome

Start date: August 2005
Phase: Phase 1/Phase 2
Study type: Interventional

To elucidate Spinal Cord Stimulation (SCS) as treatment for IBS. An SCS system with a 4-polar electrode at the T5-8 level is implanted. In a randomized, cross-over study design, active stimulation is compared to a period without stimulation, with an ensuing tailing stimulation period, twice as long. Patients recorded average pain level, pain attacks, number of diarrheas and global quality of life. At the end of the study patients can choose to retain their SCS stimulation system or have it removed. The outcome of the present trial will show whether SCS is a useful treatment of IBS. The long-term follow-up will show the continuous amelioration of SCS over at least six months.

NCT ID: NCT01726504 Completed - Constipation Clinical Trials

The Efficacy and Safety Study of Electro-acupuncture for Severe Chronic Functional Constipation

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

The main purpose of this study is to evaluate efficacy of electro-acupuncture for severe functional constipation compared with sham acupuncture, used as placebo; the secondary purpose is to evaluate the safety and post-treatment effect of electro-acupuncture.

NCT ID: NCT01722318 Completed - Clinical trials for Irritable Bowel Syndrome Characterized by Constipation

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

CIBS
Start date: November 2012
Phase: Phase 2
Study type: Interventional

This is a randomized, 12-week, double-blind, placebo-controlled, dose-ranging study in patients with IBS-C.

NCT ID: NCT01714843 Completed - Clinical trials for Constipation-predominant Irritable Bowel Syndrome (IBS-C)

A Study to Evaluate the Effect of ASP0456 in Patients With Constipation Predominant Irritable Bowel Syndrome

Start date: August 10, 2012
Phase: Phase 2
Study type: Interventional

This study is to investigate the efficacy, safety, and plasma concentration change of ASP0456 in patients with constipation-predominant irritable bowel syndrome.

NCT ID: NCT01710579 Completed - Constipation Clinical Trials

Normal Values in Ano-rectal 3D High Resolution Manometry

NOMAD
Start date: September 2012
Phase: N/A
Study type: Interventional

Ano-rectal manometry is indicative in patients with either fecal incontinence or constipation. Recently anorectal 3D- high resolution manometry has been developed. Pressure variations are measured circumferentially along the anal canal. It may allow a better understanding of anorectal disorders by displaying anal pressure asymmetry and it could be useful to assess the functional anatomy of the pelvic floor better than conventional manometry.

NCT ID: NCT01707667 Completed - Clinical trials for Chronic Constipation

Study to Investigate Prucalopride vs. Polyethylene Glycol 3350 on Colon Activity

Start date: February 27, 2013
Phase: Phase 4
Study type: Interventional

To evaluate the different effects of prucalopride and PEG 3350 + electrolytes on colon motor activity in subjects that are chronically constipated.

NCT ID: NCT01696643 Terminated - Clinical trials for Opioid-Induced Constipation

Safety Study of CB-5945 for the Treatment of Opioid-Induced Constipation

Start date: October 12, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the long-term safety and tolerability of CB-5945 for the treatment of opioid-induced constipation (OIC) in adults taking opioid therapy for chronic non-cancer pain.