Flatulence Clinical Trial
Official title:
Objective Markers Flatulence: Determination of Gas Production and Evacuation in Response to Dietary Manipulations
Background Some patients complain of excessive evacuation, which may become socially
disabling (Azpiroz F & Malagelada J-R, 2005). However, there no systematic investigation on
the range of gas evacuation in healthy subjects and in subjects complaining of flatulence
under basal conditions and in response to a high-flatulogenic diet (Azpiroz F & Levitt DG,
2009).
Hypothesis Patients complaining of excessive passage of gas per anus have more intestinal
gas production and more anal gas evacuation during basal conditions and in response to a
high flatulogenic diet than healthy subjects. This abnormality is related to the differences
in colonic microflora.
Objectives
- To determine the normal range of intestinal gas evacuation under basal conditions and
in response to a high flatulogenic diet.
- In patients complaining of flatulence, to determine whether intestinal gas evacuation
under basal conditions and in response to a high flatulogenic diet is increased.
- To identify differences in the microbiota pattern in subjects with normal and excessive
anal gas evacuation.
- In patients complaining of flatulence, to determine the segmental distribution of
intestinal gas after a diet challenge.
Methods Healthy subjects (n=20) and patients complaining of flatulence (n=30) will undergo a
3-day basal phase on their current diet and a 3-day challenge phase on a high-flatulogenic
diet; patients will be followed-up for 7 days on a low-flatulogenic diet. The following g
measurements will be performed: daily measurement of the number of anal gas passages with an
event marker, continuous recording of anal gas evacuation in the laboratory using an
electronic leakage-free gas collection system, colonic flora analysis by fecal sampling, and
segmental gas distribution in the gut by abdominal computer tomography (CT) imaging.
Relevance These studies will allow to develop the normal range of anal gas evacuation during
basal conditions. Furthermore, a provocative test will be developed for the diagnosis of
excessive gas production in patients complaining of flatulence. This data will allow a
proper diagnosis of these patients and will pave the path for a rational management and for
the development of evidence-based treatment strategies. This pilot study will allow a proper
design with adequate sample size calculation in future interventional studies.
Background Some patients complain of excessive evacuation, which may become socially
disabling (Azpiroz F & Malagelada J-R, 2005). However, the physiology and pathophysiology of
flatulence remains poorly understood (Azpiroz F & Levitt DG, 2009).
Gas evacuated by anus originates by-and-large in the colon, where unabsorbed meal residues
are fermented by colonic bacteria (Anderson et al., 1981;Levitt et al., 1987;Flourie et al.,
1988). Indeed, it has been shown that some food components are incompletely absorbed in the
small bowel and enter the colon (Wolever & Robb, 1992;Grimble, 1989;Steggerda FR,
1968;Wagner et al., 1977;Steggerda F.R. & Dimmick, 1966;Stone-Dorshow & Levitt, 1987;Wursch
et al., 1989) and that other intraluminal substrates interfere with the absorption of
nutrients (Boibin M et al., 1998;Hamberg et al., 1989;Brugge & Rosenfeld, 1987;Taylor et
al., 1986;Layer et al., 1986). Hence, the volume of gas production and anal evacuation is
determined by two main factors: the diet, particularly the amount of fermentable residues,
and the individual composition of colonic microflora. Within subjects, gas output varies in
relation to the diet (Steggerda FR, 1968;Kirk, 1949). However, there is a great
interindividual variability, and gas evacuation in subjects maintained on a similar diet may
differ substantially.
It has been shown that healthy subjects on a normal diet containing 200 g of beans evacuate
705 mL gas per 24 hours, whereas with a fiber the diet gas evacuation was 214 mL (Tomlin et
al., 1991). In healthy subjects the frequency of gas evacuation is variable, usually around
10 evacuation per day (Furne & Levitt, 1996). Based on observations on a patient that who
passed large amounts of flatus, a classification of foodstuffs depending on their gas
producing capacity was elaborated (Sutalf LO & Levitt MD, 1979). Few studies on specific
foodstuffs have been later added to complement this information (Wolever & Robb, 1992;Wagner
et al., 1977;Hickey C et al., 1972). However, there no systematic investigation on the range
of gas evacuation in healthy subjects and in subjects complaining of flatulence under basal
conditions and in response to a high-flatulogenic diet.
Procedures Recruitment questionnaire A questionnaire will be used to evaluate gas
evacuation, bowel habit and functional gut symptoms.
Daily measurement of the number of anal gas evacuations and symptoms The number of gas
evacuations per anus will be measured using an event marker during daytime. At the end of
the day the following parameters will be recorded on a questionnaire: discomfort related to
flatulence and evaluation of abdominal discomfort/pain (using 0-10 analogue scales); the
number of bowel movements and form (using the Bristol scale; (Heaton & O'Donnell, 1994) and
gastrointestinal well-being (satisfaction/dissatisfaction using a 10 point scale graded from
+5 to -5).
Analysis of colonic flora The composition of the intestinal flora will be evaluated
measuring flora composition in stools. Subjects will be supplied with two Stool Collecting
Kits (each containing two weighed sampling tubes containing RNA synthesis stabilization
buffers (RNA later, Ambion), one of which is a spare) into which they will provide a small
sample of their stool (at least 30g). After mixing the stool with the buffer in the supplied
tube, subjects will store the tubes in the box at home until they next visit at the
hospital, where it will be centrifuged at 12000rpm for 5 minutes, supernatant removed and
fecal pellet stored at - 80oC in the Gastroenterology Research Unit. Samples will be
transported to Danone Research, France where they will be analysed for composition of
intestinal flora (bacteria).
Using molecular based methods, the concentration of dominant and some sub-dominant bacterial
groups of intestinal flora will be measured. These include bacteria that belong to
Actinobacteria, Bacteroidetes, Firmicutes, Fusobacteria, Proteobacteria, Euryarcheota
groups.
Continuous recording of anal gas evacuation Participants will be studied in the laboratory.
After a standard breakfast, rectal gas will be collected via a rectal cannula. Anal gas will
be collected via a leak proof, low resistance collection line, using a barostat and the
volume will be continuously recorded for either 3 or 8 hours (see study design). The
composition of the gas collected will be analyzed.
Once the subjects are positioned in bed, a non-stretch belt, 48 mm wide, with a metric scale
will be adjusted around the abdomen by means of two elastic bands. All girth changes will be
measured while the subjects are breathing relaxed, and will be referenced to the mid point
of respiratory displacements.
A graded questionnaire will be used to measure the intensity and the type of sensations
perceived, and an anatomical questionnaire to measure the location and extension of the
perceived sensations. The graded questionnaire includes five visual analogue scales graded
from 0 (no perception) to 6 (pain), specifically for scoring: a) sensation of increased
abdominal pressure, b) sensation of abdominal distension, c) colicky/rumbling sensation, d)
puncture/stinging sensation, and d) other type of sensation (to be specified by the
participant in the questionnaire), respectively. The questionnaire includes two additional
scales for scoring feeling of difficult evacuation of gas per anus, and belching,
respectively, that will be analyzed separately. Subjects will be asked to score any
perceived sensation (one or more perceived simultaneously) on the scales. The anatomical
questionnaire incorporates a diagram of the abdomen divided in nine regions corresponding to
epigastrium, periumbilical area, hypogastrium, both hypochondria, flanks, and ileal fossae.
Subjects will be instructed to mark the location, i.e., abdominal region (s) or
extraabdominal, where the sensations are perceived.
Segmental gas distribution in the gut In patients complaining of bloating, an abdominal CT
scan will be taken. This scan will be used to rule out organic disorders. Furthermore, using
an original program, abdominal morpho-volumetric analysis will be performed to measure gas
volumes in different gut. All female participants with childbearing potential will undergo a
urine pregnancy test 24 hours prior to the scan.
Hyperflatulogenic diet challenge For 3 days participants will be asked to consume a diet
rich in fermentable residues to increase their gas production rate.
Low-flatulogenic diet At the end of the study, patients will be put on a low residue diet
for 7 days; this will give an indication of the potentially expected response to treatment.
Working Plan Each subject will attend the following visits; the first recruitment visit will
be performed by the attending physician in the outpatient clinic, and the rest, including
the physiological measurements in the Digestive System Research Unit; CT imaging will be
performed in the Department of Radiology.
Visit 1. Recruitment: entry questionnaires. Visit 2. Before basal period: instructions,
informed consent, and delivery of event marker, questionnaires, and material for fecal
sampling.
Visit 3. Last day of basal phase. Continuous recording of anal gas evacuation. Delivery of
dietary instructions (high-flatulogenic diet) and questionnaires. In 8 patients segmental
gas distribution will be also measured during the basal phase.
Visit 4. Last day of challenge phase. Continuous recording of anal gas evacuation. CT for
evaluation of segmental gas distribution in the gut. In patients only: delivery of dietary
instructions (low-flatulogenic diet) and questionnaires.
Visit 5. Last day of correction phase. In patients only: collection of data and materials.
;
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening
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