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Effect of Psyllium (Plantago Ovata) on Digestive Disorders in Familial Amyloidosis (Psyllium)

Primary Purpose

Familial Amyloidosis

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Psyllium
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Familial Amyloidosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • male or female age ≥ 18
  • suffering from familial amyloidosis confirmed by: i) the presence of a specific mutation in transthytetin gene and/or ii) amyloid deposits immunostained for transthyretin in a tissue biopsy
  • stage 1 or 2 on the familial amyloid polyneuropathy scale
  • receiving a stable dose for at least 3 months if treated with Patisaran® and inotersen (Tegsedi®),
  • suffering from gastro intestinal pain ≥ 4 on Visual Analog Scoale (VSA)
  • affiliated to social security
  • able to understand the inform consent form
  • if women of child bearing age, using an effective birth control method for the period of study participation

Exclusion criteria:

  • allergic to Psyllium
  • intestinal or esophageal stenosis or any other type of real or suspected gastrointestinal obstruction
  • protection by law under guardianship, or who cannot participate in a clinical study under Article L. 1121-16 of the French Code of Public Health
  • participation in the last 3 months in a clinical research study in which he / she has been exposed to a pharmaceutical product or a medical device
  • treatment with tafamidis (Vyndaqel®)
  • concomitant intake of food supplements containing zinc, iron, calcium, magnesium or vitamin B12,
  • contraindication to taking Psyllium, e.g. fecal impaction, gastrointestinal obstruction, esophageal or intestinal stenosis or dysphagia to liquids
  • stage 0 or 3 on the familial amyloid polyneuropathy scale
  • pregnant or breastfeeding female patient (a urine pregnancy test will be performed for women of childbearing age)
  • any pathology or concomitant treatment that may interfere with the progress of the study.

Sites / Locations

  • University Hospital of NiceRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Familial amyloidosis patients

Arm Description

Familial amyloidosis patients with gastro-intestinal pain receiving Psyllium

Outcomes

Primary Outcome Measures

Effect of Psyllium administration on digestive quality of life in familial amyloidosis patients
The effect of Psyllium administration on digestive quality of life in familial amyloidosis patients will be evaluated at 6 months using the Gastrointestinal Quality of Life index (GIQLI)

Secondary Outcome Measures

Effect of Psyllium administration on global quality of life in familial amyloidosis patients
The effect of Psyllium administration on global quality of life in familial amyloidosis patients will be evaluated at 6 months using the Norfolk Quality of Life - questionnaire
Effect of Psyllium administration on motor function in familial amyloidosis patients
The effect of Psyllium administration on motor function in familial amyloidosis patients will be evaluated at 6 months using the Neuropathy Impairment Score Lower Limb tests (0 to 88; 0 is defined as a normal status)
Effect of Psyllium administration on gastro intestinal pain in familial amyloidosis patients
The effect of Psyllium administration on gastro intestinal pain in familial amyloidosis patients will be evaluated at 6 months using the visual analogy scale (0 to 10; 0 is defined as no pain status)
Effect of Psyllium administration on stool density in familial amyloidosis patients
The effect of Psyllium administration on stool density in familial amyloidosis patients will be evaluated at 6 months using the Bristol score (1 to 7; 1-2 is defined as a constipation status, 3-4 is the most regular status, 5-7 is defined by diarrheas)
Adverse effects of Psyllium administration in familial amyloidosis patients
Adverse effects of Psyllium administration in familial amyloidosis patients will be recorded thoughout the study

Full Information

First Posted
January 4, 2021
Last Updated
August 2, 2023
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT04695340
Brief Title
Effect of Psyllium (Plantago Ovata) on Digestive Disorders in Familial Amyloidosis
Acronym
Psyllium
Official Title
Effect of Psyllium (Plantago Ovata) on Digestive Disorders in Familial Amyloidosis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 2023 (Anticipated)
Primary Completion Date
May 2025 (Anticipated)
Study Completion Date
May 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Familial amyloidosis is a rare disease that mainly affects the nerves and heart, but also more rarely the eyes and kidneys. This disease is due to a mutation in the gene encoding the synthesis of transthyretin, resulting in a modification of the translated protein. This abnormal protein and its derivatives are deposited in the form of a toxic "amyloid" substance in tissues and organs, altering their functions, particularly in the gastrointestinal tract. From a gastrointestinal perspective, different treatments can be proposed in the absence of specific recommendations for familial amyloidosis. The hygienic and dietary measures consist of avoiding tobacco, alcohol and carbonated drinks, limiting fatty meals rich in poorly digestible fibers, and splitting meals. If this fails, metoclopramide and domperidone are suggested. As a second-line erythromycin, can be used with caution because of cardiac risks and drug interactions. Polyethylene glycol-based osmotic laxatives can be used to treat constipation. Alternating diarrhea and constipation can be treated with ispaghul-based laxatives, aiming at transit regulation. Finally, refractory diarrhea can be treated with the administration of loperamide. If this fails, treatment with a somatostatin analogue may be offered. However, all these treatments can present significant side effects, therefore natural alternatives are often sought. Psyllium in particular regulates transit by normalizing stool consistency: it is effective against digestive disorders such as constipation, but it is also effective in the event of diarrhea. It allows the formation of a viscous gel by the hydrophilicity of polysaccharides macromolecules, increasing the fecal bowl which stimulates peristalsis and facilitates defecation. The WHO has recognized that Psyllium is superior to wheat bran in the treatment of irritable bowel syndrome. The main objective of the study is to assess the effect of daily Psyllium administration on digestive quality of life in familial amyloidosis patients who suffer from digestive disorders.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Familial Amyloidosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Familial amyloidosis patients
Arm Type
Experimental
Arm Description
Familial amyloidosis patients with gastro-intestinal pain receiving Psyllium
Intervention Type
Dietary Supplement
Intervention Name(s)
Psyllium
Intervention Description
Psyllium is given to patients
Primary Outcome Measure Information:
Title
Effect of Psyllium administration on digestive quality of life in familial amyloidosis patients
Description
The effect of Psyllium administration on digestive quality of life in familial amyloidosis patients will be evaluated at 6 months using the Gastrointestinal Quality of Life index (GIQLI)
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Effect of Psyllium administration on global quality of life in familial amyloidosis patients
Description
The effect of Psyllium administration on global quality of life in familial amyloidosis patients will be evaluated at 6 months using the Norfolk Quality of Life - questionnaire
Time Frame
6 months
Title
Effect of Psyllium administration on motor function in familial amyloidosis patients
Description
The effect of Psyllium administration on motor function in familial amyloidosis patients will be evaluated at 6 months using the Neuropathy Impairment Score Lower Limb tests (0 to 88; 0 is defined as a normal status)
Time Frame
6 months
Title
Effect of Psyllium administration on gastro intestinal pain in familial amyloidosis patients
Description
The effect of Psyllium administration on gastro intestinal pain in familial amyloidosis patients will be evaluated at 6 months using the visual analogy scale (0 to 10; 0 is defined as no pain status)
Time Frame
6 months
Title
Effect of Psyllium administration on stool density in familial amyloidosis patients
Description
The effect of Psyllium administration on stool density in familial amyloidosis patients will be evaluated at 6 months using the Bristol score (1 to 7; 1-2 is defined as a constipation status, 3-4 is the most regular status, 5-7 is defined by diarrheas)
Time Frame
6 months
Title
Adverse effects of Psyllium administration in familial amyloidosis patients
Description
Adverse effects of Psyllium administration in familial amyloidosis patients will be recorded thoughout the study
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: male or female age ≥ 18 suffering from familial amyloidosis confirmed by: i) the presence of a specific mutation in transthytetin gene and/or ii) amyloid deposits immunostained for transthyretin in a tissue biopsy stage 1 or 2 on the familial amyloid polyneuropathy scale receiving a stable dose for at least 3 months if treated with Patisaran® and inotersen (Tegsedi®), suffering from gastro intestinal pain ≥ 4 on Visual Analog Scoale (VSA) affiliated to social security able to understand the inform consent form if women of child bearing age, using an effective birth control method for the period of study participation Exclusion criteria: allergic to Psyllium intestinal or esophageal stenosis or any other type of real or suspected gastrointestinal obstruction protection by law under guardianship, or who cannot participate in a clinical study under Article L. 1121-16 of the French Code of Public Health participation in the last 3 months in a clinical research study in which he / she has been exposed to a pharmaceutical product or a medical device treatment with tafamidis (Vyndaqel®) concomitant intake of food supplements containing zinc, iron, calcium, magnesium or vitamin B12, contraindication to taking Psyllium, e.g. fecal impaction, gastrointestinal obstruction, esophageal or intestinal stenosis or dysphagia to liquids stage 0 or 3 on the familial amyloid polyneuropathy scale pregnant or breastfeeding female patient (a urine pregnancy test will be performed for women of childbearing age) any pathology or concomitant treatment that may interfere with the progress of the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michel CAVALLI
Phone
0492035753
Ext
+33
Email
cavalli.m@chu-nice.fr
Facility Information:
Facility Name
University Hospital of Nice
City
Nice
State/Province
Provence Alpes Cote d'Azur
ZIP/Postal Code
06000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michel CAVALLI
Phone
0492035753
Ext
+33
Email
cavalli.m@chu-nce.fr
First Name & Middle Initial & Last Name & Degree
Sabrina Sacconi, Pr
First Name & Middle Initial & Last Name & Degree
Michel CAVALLI
First Name & Middle Initial & Last Name & Degree
Andra EZARU

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effect of Psyllium (Plantago Ovata) on Digestive Disorders in Familial Amyloidosis

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