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Constipation clinical trials

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NCT ID: NCT00912301 Completed - Clinical trials for Constipation-predominant Irritable Bowel Syndrome

Cheno Effect on Transit in Health and IBS-C

Chenotransit
Start date: April 2009
Phase: Phase 2
Study type: Interventional

The study hypothesis is that the naturally occurring bile acid, chenodeoxycholic acid, induces acceleration of colonic transit in health and in patients with constipation-predominant Irritable Bowel Syndrome (IBS-C).

NCT ID: NCT00909116 Completed - Constipation Clinical Trials

International Multicenter Prospective Transtar Registry

Start date: January 31, 2009
Phase: N/A
Study type: Observational

Obstructed Defecation Syndrome (ODS) describes a condition which is characterized by chronic constipation. The symptoms of ODS include abdominal pain or cramping, irregular bowel frequency and the feeling of not having emptied the rectum. ODS is usually associated with internal rectal prolapse and/or rectocele. For surgical treatment of ODS, a plethora of surgical techniques have been described with no one method having been assessed as a gold standard.

NCT ID: NCT00908076 Completed - Parkinson's Disease Clinical Trials

Amitiza in Constipation Associated With PD (Parkinson's Disease)

AMITIZA
Start date: February 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if Amitiza (lubiprostone), a drug proven to be safe and effective for chronic constipation, will also improve constipation symptoms in Parkinson's Disease patients. We will also evaluate the impact of the drug on changes in bowel movement consistency, quality of life and motor symptoms.

NCT ID: NCT00906971 Completed - Clinical trials for Chronic Constipation

Physiotherapeutic Intervention in Children With Chronic Functional Constipation

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether physiotherapy is effective in the treatment of the chronic functional constipation in children.

NCT ID: NCT00903747 Completed - Constipation Clinical Trials

Thorough Corrected QT Interval (QTc) Study To Evaluate Possible Effects of Prucalopride on ECG Parameters

Start date: January 2009
Phase: Phase 1
Study type: Interventional

This is a 2-arm, parallel-group active- and placebo-controlled, double-blind randomised study, stratified by gender and with a hybrid crossover group design, to compare treatment with prucalopride 2 mg/day (intended therapeutic dose) and prucalopride 10 mg/day (supratherapeutic dose) with placebo. A single oral dose of 400 mg moxifloxacin is included as a positive control in terms of the effect on cardiac repolarisation. Study hypothesis: Treatment with therapeutic (2 mg) or supratherapeutic (10 mg) doses of prucalopride in healthy male and female volunteers will not increase QTc interval compared to placebo.

NCT ID: NCT00902837 Completed - Clinical trials for Chronic Osteoarthritis

OXN PR Compared to OxyPR to Demonstrate Non-inferiority in Pain & Locomotor Function & Improvement in Symptoms of Constipation in OA Subjects

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The primary objectives are - to demonstrate that the treatment with OXN PR tablets is non-inferior to the treatment with OxyPR with regards to analgesic efficacy and locomotor function. - to demonstrate that subjects with moderate to severe OA pain taking oxycodone/naloxone prolonged release tablets have improvement in symptoms of constipation compared to subjects taking oxycodone prolonged release tablets alone

NCT ID: NCT00902031 Completed - Constipation Clinical Trials

Effectiveness of Docusate in Preventing/Treating Constipation in Palliative Care Patients

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

The purpose of this study is to determine if docusate is effective in the treatment of constipation in palliative care patients.

NCT ID: NCT00892086 Recruiting - Depression Clinical Trials

Prevalence and Recognition of Geriatric Syndrome in Outpatient Clinic at Srinagarind Hospital

Start date: May 2009
Phase: N/A
Study type: Observational

The purpose of this study is to collect the prevalence of geriatric syndrome, which is recognized by an internist, and to compare the data based on the comprehensive geriatric assessment by a geriatrician. The secondary outcome is to develop a practical collected form for the internist.

NCT ID: NCT00888147 Completed - Constipation Clinical Trials

Fiber Formula Study Among Radiation Oncology Patients

Start date: April 2009
Phase: N/A
Study type: Observational

During radiation treatment for head and neck cancer a large percentage of patients at Mayo Clinic Rochester develop the need for tube feeding to meet nutrition and hydration needs. These patients are usually taking pain medication along with a stool softener or laxative. Currently, when these patients get a feeding tube it is our standard practice to choose a fiber-free enteral tube feeding formula as to not worsen their constipation. Currently, there are no guidelines as to which patients are good candidates for fiber containing enteral tube feeding formulas. The investigators hope this study will help determine if fiber containing enteral tube feeding formulas can be used for patients undergoing radiation for head and neck cancer without increasing rates of constipation or increasing use of stool softeners/laxatives. Hypothesis: Participants enrolled in the study will not have increased rates of constipation on fiber-containing enteral tube feeding formula compared to historical standards on fiber-free formula.

NCT ID: NCT00872430 Completed - Clinical trials for Chronic Constipation

Laxative Effectiveness of a Phytotherapeutic Tea

Start date: July 2002
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate the efficacy and safety of a phytotherapeutic laxative tea, composed by Pimpinella anisum, Foeniculum vulgare, Sambucus nigra and Cassia angustifolia, in a randomized crossover placebo-controlled clinical trial in patients with chronic constipation.