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Constipation clinical trials

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NCT ID: NCT00746200 Completed - Clinical trials for Chronic Constipation

Acupuncture for Chronic Constipation

Start date: October 2008
Phase: Phase 3
Study type: Interventional

Since there have been few advances for constipation in laxative treatment in the last 50 years, this study is designed to evaluate the efficacy and safety of acupuncture for patients with chronic constipation based on the theory of traditional Chinese Medicine.

NCT ID: NCT00745147 Completed - Clinical trials for Chronic Constipation

Comparison of TCM and Laxatives for Adults With Chronic Constipation

Start date: July 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare the therapeutic efficacy, safety, cost-effectiveness and maintenance effect between Chinese herbal formula and lactulose on chronic constipation in long-term care.

NCT ID: NCT00742872 Terminated - Clinical trials for Constipation-Predominant Irritable Bowel Syndrome

Randomized Trial of Mosapride Versus Placebo in the Treatment of Constipation-Predominant Irritable Bowel Syndrome

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether Mosapride, an agent which acts on serotonin receptors in the gastrointestinal tract, is effective in the treatment of constipation-predominant irritable bowel syndrome (C-IBS).

NCT ID: NCT00741936 Completed - Constipation Clinical Trials

An Effectiveness and Safety Study of Chinese Herbal Medicine for Functional Constipation

Start date: July 2008
Phase: Phase 2
Study type: Interventional

Functional constipation (FC) is a common complaint in clinical practice, but treatment for this condition in conventional medicine is suboptimal. Complementary and alternative medicines, especially Chinese herbal medicine (CHM) are used frequently by patients, however, there is little research evidence about these commonly used CHM. The purpose of the study is evaluate the efficacy and safety of an ancient CHM formula, MaZiRenWan (MZRW), by comparing with placebo.

NCT ID: NCT00735605 Completed - Constipation Clinical Trials

Comparative Study Between Surgical and Non Surgical Treatment of Anismus in Patients

Start date: September 2006
Phase: N/A
Study type: Interventional

Comparative study between surgical and non surgical treatment of anismus in patients with symptoms of obstructed defecation. Anismus is a significant cause of chronic constipation. This study came to compare the results of BFB training , BTX-A injection and PDPR in the treatment of anismus patients. Patients and methods: Seventy two anismus patients fulfilled Rome II criteria for functional constipation were included in this study. All patients underwent anorectal manometry, balloon expulsion test, defecography, and electromyography activity of the EAS. All patients had non relaxing puborectalis muscle.. The patients were randomized into three groups. Group I patients received biofeedback therapy, two times per week for about 1 month. Group II patients were injected with BTX- A. Group 111 partial division of puborectalis was done. Follow up was conducted weekly in the first month then monthly for about 1 year.

NCT ID: NCT00730171 Completed - Clinical trials for Chronic Constipation

An Open-label, Long-term Safety Study of Linaclotide in Patients With Chronic Constipation or Irritable Bowel Syndrome With Constipation

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The objective of this study is to assess the long-term safety of linaclotide administered to patients with chronic constipation (CC) or irritable bowel syndrome with constipation (IBS-C).

NCT ID: NCT00730015 Completed - Clinical trials for Chronic Constipation

Trial of Linaclotide in Patients With Chronic Constipation

Start date: August 2008
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 constipation (CC). 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: NCT00728975 Completed - Constipation Clinical Trials

The Bowel Research Collaborative Data Tracking System Implementation Study

Start date: June 2008
Phase:
Study type: Observational

The project's primary purpose is to establish a network of Hospice Palliative Care settings using a common and consistent method of assessing and documenting bowel functioning in order to be able to carry out future collaborative studies of constipation treatments. The secondary goal is to gather normative data on current bowel care function and outcomes of current treatments which can be used to determine sample size calculations for future controlled trials of bowel management protocols. In order to complete this goal the project requires a thorough assessment of current nursing practice in regard to bowel care.

NCT ID: NCT00712543 Completed - Constipation Clinical Trials

A Preference Study Comparing Kristalose® and Liquid Lactulose

Start date: June 2009
Phase: Phase 4
Study type: Interventional

This study will evaluate whether patients have an overall preference for Kristalose® or liquid lactulose based on taste, consistency, and portability.

NCT ID: NCT00706004 Completed - Cystic Fibrosis Clinical Trials

Short Term Safety and Efficacy of Lubiprostone in Adults With Cystic Fibrosis

Start date: July 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the short term safety and effectiveness of lubiprostone when used for constipation in adults with cystic fibrosis.