Prove of Concept Study, to Evaluate the Efficacy, Safety, and Tolerability of IBEROGAST in the Treatment of Bowel Troubles in Patients With Parkinson's Disease
NCT ID: NCT02719496
Last Updated: 2018-04-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE2
45 participants
INTERVENTIONAL
2016-04-30
2018-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
A Proof of Concept Study of Pradigastat in Patients With Functional Constipation
NCT04620161
Efficacy and Safety of Lubiprostone in the Treatment of Slow Transit Constipation
NCT07277907
Lubiprostone, Colonic Motility and Sensation
NCT00953043
Lubiprostone for Treatment of Chronic Idiopathic Constipation
NCT02695719
Study of Comparative Effectiveness of Prucalopride and Lubiprostone in Constipation Predominant Irritable Bowel Syndrome
NCT04985669
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
IBEROGAST
Dose of 20 drops three times a day for 28 days, on constipation parkinsonian patients with disorders intestinal transit.
IBEROGAST
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
IBEROGAST
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Parkinson's disease according to the criteria of the United Kingdom Parkinson's Disease Society Brain Bank
* Presence of constipation defined by the Rome III criteria Functional constipation
* Social assured Patient
* Patients with signed consent
Exclusion Criteria
* Constipation Drug
* Other neurological disorder Parkinson's disease
* Metabolic disease diabetes collagenoses
* Severe renal or hepatic impairment
* Pregnant or lactating women
* Premenopausal women without contraceptive device effective
* Regular and prolonged use of history (\> 12 months) of laxatives irritants
* Use of oral laxative treatment in the two weeks before the start of treatment, and refusal to stop these treatment during the course of the study
* Taking treatment antabuse
* Cognitive impairment compromising understanding or application instructions
* Patient already included in a research protocol
* Minors
* Nobody protected by law
30 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Nantes University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Tiphaine Rouaud
Nantes, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RC15_0396
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.