Clinical Trials Directory

Trials / Completed

CompletedNCT01637857

Oligo-antigenic Diet in the Treatment of Chronic Anal Fissures.

Oligo-antigenic Diet in the Treatment of Chronic Anal Fissures. Evidence for a Relationship Between Food Hypersensitivity and Anal Fissures

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
161 (actual)
Sponsor
University of Palermo · Academic / Other
Sex
All
Age
17 Years
Healthy volunteers
Not accepted

Summary

Patients with chronic constipation due to food hypersensitivity (FH) had an elevated anal sphincter resting pressure. No studies have investigated a possible role of FH in anal fissures (AF). We aim to evaluate the effectiveness of a diet in curing AF and the clinical effects of a double-blind placebo controlled (DBPC) challenge with cow's milk protein or wheat.

Detailed description

Context: Patients with chronic constipation due to food hypersensitivity (FH) had an elevated anal sphincter resting pressure. No studies have investigated a possible role of FH in anal fissures (AF). Objective: We aim to evaluate 1) the effectiveness of a diet in curing AF; 2) the clinical effects of a double-blind placebo controlled (DBPC) challenge with cow's milk protein or wheat. Design: The study will have two different parts: the first to verify the effectiveness of the oligo-antigenic diet in chronic AF treatment; the second to search for a possible cause-effect relationship between the diet and the onset of the AF. Setting: We will enrol consecutive adult patients with chronic AF who will refer to a Surgical Department of the University of Palermo for a 3-years period. Inclusion criteria are: evidence of CAF evaluated by an experienced rectal surgeon; patient age \>16 years. Exclusion criteria are: a diagnosis of inflammatory bowel disease, ongoing steroid treatment performed for any reason, an exclusion diet followed for any reason, and pregnancy. At the time of the first evaluation, routine laboratory tests, immunology tests, rectal biopsies and anal-rectal manometry will be performed. Patients: patients, finally included in the study, will be randomized to one of the treatment groups. Interventions: Enrolled patients will be randomized to receive a "true elimination diet" or a "sham elimination diet"; both groups will also receive topical nifedipine and lidocaine. Main Outcome Measures: The patients will be evaluated every two weeks for CAF persistence or healing; anal pain will be scored on a visual analogue scale ranging from 0 (absence of pain) to 10 (intolerable pain). Anal-rectal manometry will be repeated at the end of the study period, in all patients who will be treated.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTsham oligoantigenic diet associated to lifestyle instructionsham oligoantigenic diet associated to lifestyle instruction
DIETARY_SUPPLEMENToligoantigenic dietoligoantigenic diet associated to life style counseling

Timeline

Start date
2006-01-01
Primary completion
2009-12-01
Completion
2010-12-01
First posted
2012-07-11
Last updated
2013-01-11

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01637857. Inclusion in this directory is not an endorsement.