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Occult Obscure Gastrointestinal Bleeding (OGIB)

B

Blymum

Status

Completed

Conditions

Gastrointestinal Bleeding

Treatments

Dietary Supplement: PG low molecular weight chitosan

Study type

Interventional

Funder types

Other

Identifiers

NCT03464539
20180206_UC

Details and patient eligibility

About

To test the activity of a polyglucosamine (PG) together with a Standard Management protocol (SM) on the occult and obscure gastrointestinal bleeding (OGIB) and the clinical symptoms in patients suffering from colonic diverticulitis (CD).

Full description

The trial was conducted in a single center and subjects were participating to the San Valentino Vascular Screening Project (SVVSP). Sixty patients with history of colonic diverticulitis (CD) and occult obscure gastrointestinal bleeding (OGIB) were recruited. All subjects were following a Standard Management (SM) protocol consisting of diet and lifestyle modifications, and were freely choosing to be treated with polyglucosamine (PG) or to follow the SM only. Two groups of 30 cases each were formed and followed for 3 months.

Diet was controlled three times (baseline and during the first and third month), through the Food Intake Assessment (FIA) which consisted of the weekly analysis of 25 different servings (e,g fruits, vegetables, pulses, first dish, meat, processed meat, cheese). The lifestyle modification consisted of physical exercise (9 MET (Metabolic Equivalents) -h/week of brisk walking) and oral hygiene.

The main variable was OGIB, that was measured using Hemoccult Sensa Fecal Occult Blood Procedure.

Ancillary variables where the hs-CRP (high sensitivity C Ractive Protein) and the daily gastrointestinal discomfort (GID) measured thorough a visual analogue scale (VAS) from 0 to 10.

All variables were taken at baseline, after one and three months with the exception of GID that was measured also after one week of treatment.

Enrollment

60 patients

Sex

All

Ages

55 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects aged between 55 to 65 years (males and females).
  • CD diagnosis.
  • DICA (Diverticular Inflammation and Complication Assessment) class DICA 2 or DICA 3.
  • OGIB positive to Hemoccult Sensa Fecal Occult Blood Procedure.

Exclusion criteria

  • Subjects with Class DICA > 3.
  • Therapy with mesalazine antibiotics and probiotics.
  • Cancer of any type (a part from benign polyposis),
  • Alcoholism.
  • Parkinsonism.
  • Alzheimer's Disease.
  • Severe depression.
  • Drug addiction.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

CD patients
Other group
Description:
PG low molecular weight chitosan 3 times per day
Treatment:
Dietary Supplement: PG low molecular weight chitosan

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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