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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 (PHYTOPARK)

Primary Purpose

Gastrointestinal Disorders in Parkinson's Disease

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
IBEROGAST
Sponsored by
Nantes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastrointestinal Disorders in Parkinson's Disease

Eligibility Criteria

30 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient 30 to 80 years
  • 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:

  • Organic Affection colic
  • 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

Sites / Locations

  • Tiphaine Rouaud

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

IBEROGAST

Arm Description

Dose of 20 drops three times a day for 28 days, on constipation parkinsonian patients with disorders intestinal transit.

Outcomes

Primary Outcome Measures

increasing the weekly number of exemptions of 3 in the last week of treatment compared with the reference week (Efficacity)
evaluate the efficacy of Iberogast, over a 28-day period, for the treatment of constipation in parkinsonian patients suffering from gastrointestinal disorders.

Secondary Outcome Measures

quality of evacuations
weekly percentage defecation requiring thrusts, or accompanied by a sensation of incomplete rectal evacuation (agenda stool), shape and consistency of stools (Bristol scale).
Gastrointestinal Symptom Rating Scale (quality of life)
the impact of gastrointestinal symptoms on quality of life measured by the Gastrointestinal Symptom Rating Scale
Short Form Health Survey (SF36) (quality of life)
the impact of gastrointestinal symptoms on quality of life measured by the Short Form Health Survey (SF36)
use of rectal laxatives
use of rectal laxatives (stool diary)
clinical global improvement of gastrointestinal symptoms
Patient Global Impression of Change
motor and non-motor symptoms
Movement Disorder Society - Unified Parkinson Disease Rating Scale
Parkinson Disease Quotation ( PDQ39) (tolerability in parkinsonian)
Parkinson Disease Quotation ( PDQ39)
Incidence of Treatment-Emergent Adverse Events (Tolerability)
adverse event reporting

Full Information

First Posted
March 15, 2016
Last Updated
April 20, 2018
Sponsor
Nantes University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02719496
Brief Title
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
Acronym
PHYTOPARK
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
April 2016 (undefined)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
April 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nantes University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of this study is to evaluate the efficacy of STW5 Iberogast, over a 28-day period, for the treatment of constipation in parkinsonian patients suffering from gastrointestinal disorders.
Detailed Description
Gastrointestinal disorders are the most common non-motor symptoms of Parkinson's disease (PD). They affect the entire intestinal tract and include excess saliva stasis (70% of patients), dysphagia (52%), gastroparesis (34-45%), and constipation. Gastroparesis participates in dyspepsia and abdominal pain. Constipation, as defined by the international standards criteria of Rome III, is present in 59% of PD patients and leads to functional impairment in 70% of patients. The mechanism underlying constipation is multifactorial and may include slow transit and defecation disorders secondary to anorectal dysfunction. Bowel disorders are present in the early stage of the disease and usually precede the onset of motor symptoms. They may result from lesions of the enteric nervous system, of the autonomic nervous system, and from probable alterations in gastrointestinal motility controlled by the central nervous system. The STW5 (Iberogast, Steigerwald, Germany) is a herbal agent composed of nine plant extracts, with prokinetic, antispasmodic, prosecretory, anti-inflammatory and anti-oxidant properties. These properties have been demonstrated in animals and in human pathology, in the treatment of dyspepsia and irritable bowel syndrome. It is the only phytotherapeutic agent which efficacy was demonstrated by randomized double-blind trials in these indications. In PD, the STW5 could improve constipation due to its prokinetic effects of the prosecretory enteric neurons. It could also improve dyspepsia and abdominal pain by its antispasmodic properties. We propose to study the efficacy and the safety of STW5 on bowel dysfunction in parkinsonian patients, especially on constipation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastrointestinal Disorders in Parkinson's Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
IBEROGAST
Arm Type
Experimental
Arm Description
Dose of 20 drops three times a day for 28 days, on constipation parkinsonian patients with disorders intestinal transit.
Intervention Type
Drug
Intervention Name(s)
IBEROGAST
Primary Outcome Measure Information:
Title
increasing the weekly number of exemptions of 3 in the last week of treatment compared with the reference week (Efficacity)
Description
evaluate the efficacy of Iberogast, over a 28-day period, for the treatment of constipation in parkinsonian patients suffering from gastrointestinal disorders.
Time Frame
28 days
Secondary Outcome Measure Information:
Title
quality of evacuations
Description
weekly percentage defecation requiring thrusts, or accompanied by a sensation of incomplete rectal evacuation (agenda stool), shape and consistency of stools (Bristol scale).
Time Frame
28 days
Title
Gastrointestinal Symptom Rating Scale (quality of life)
Description
the impact of gastrointestinal symptoms on quality of life measured by the Gastrointestinal Symptom Rating Scale
Time Frame
28 days
Title
Short Form Health Survey (SF36) (quality of life)
Description
the impact of gastrointestinal symptoms on quality of life measured by the Short Form Health Survey (SF36)
Time Frame
28 days
Title
use of rectal laxatives
Description
use of rectal laxatives (stool diary)
Time Frame
28 days
Title
clinical global improvement of gastrointestinal symptoms
Description
Patient Global Impression of Change
Time Frame
28 days
Title
motor and non-motor symptoms
Description
Movement Disorder Society - Unified Parkinson Disease Rating Scale
Time Frame
28 days
Title
Parkinson Disease Quotation ( PDQ39) (tolerability in parkinsonian)
Description
Parkinson Disease Quotation ( PDQ39)
Time Frame
28 days
Title
Incidence of Treatment-Emergent Adverse Events (Tolerability)
Description
adverse event reporting
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient 30 to 80 years 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: Organic Affection colic 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
Facility Information:
Facility Name
Tiphaine Rouaud
City
Nantes
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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