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Monocultivar Coratina Extra Virgin Olive Oil in UC Patients (EVORCU)

Primary Purpose

Ulcerative Colitis Chronic Mild

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Beclomethasone dipropionate in addition to MC-EVOO
Beclomethasone dipropionate in addition to refined oil
Sponsored by
Casa Sollievo della Sofferenza IRCCS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Ulcerative Colitis Chronic Mild focused on measuring Ulcerative colitis, UC, Extra virgin olive oil, Polyphenols

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with active UC (diagnosed for at least 3 months) aged 18 to 70 years
  • Patients with mild to moderate disease (calculated by Mayo score).
  • Patients can provide their informed consent to participate in the study

Exclusion Criteria:

  • Patients with Crohn's disease
  • Patients with complicated disease, who are candidates for urgent surgery
  • Patients with colostomy
  • Patients with contraindications to steroid therapy (diabetes mellitus, severe osteoporosis, vertebral fractures, previous intolerance to steroid therapy)
  • Patients with unstable or inappropriately controlled cardiovascular, pulmonary, hepatic, renal or hematologic diseases
  • Patients who are not compliant
  • Patients abusing alcohol or drugs

Sites / Locations

  • IRCCS Casa Sollievo della SofferenzaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

MC-EVOO in addition to steroid therapy

Refined olive oil and steroid therapy

Arm Description

Oral beclomethasone dipropionate at dose of 10 mg / day for the first 4 weeks, 5 mg / day for the second 4 weeks plus MC- EVOO for 12 weeks at a dose of 2 tablespoons per day (1 before lunch and 1 before dinner). Each spoon will contain 10 grams of oil containing 5 mg of biophenols.

Oral beclomethasone dipropionate (10 mg / day for the first 4 weeks, 5 mg / day for the second 4 weeks) plus placebo consisting of refined olive oil with low biophenols.

Outcomes

Primary Outcome Measures

Evaluation of the short-term clinical response
Evaluation of the short-term clinical response rate in the 2 treatment groups

Secondary Outcome Measures

Evaluation of the clinical remission
Evaluation of the clinical remission rate in the short term in the 2 treatment groups
Evaluation of the endoscopic remission
Evaluation of the endoscopic remission rate after 3 months in the 2 treatment groups
Evaluation of markers of inflammation
Evaluation of the rate of patients with normalization of markers of inflammation in the short and medium term in the 2 treatment groups
Evaluation of adverse events
Evaluation of the rate of adverse events in the 2 treatment groups

Full Information

First Posted
November 24, 2017
Last Updated
February 5, 2018
Sponsor
Casa Sollievo della Sofferenza IRCCS
Collaborators
Fondazione Schena
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1. Study Identification

Unique Protocol Identification Number
NCT03408847
Brief Title
Monocultivar Coratina Extra Virgin Olive Oil in UC Patients
Acronym
EVORCU
Official Title
Supplementation of Extra Virgin Olive Oil Monocultivar Coratina in Patients With Active Ulcerative Colitis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 20, 2017 (Actual)
Primary Completion Date
December 1, 2018 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Casa Sollievo della Sofferenza IRCCS
Collaborators
Fondazione Schena

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Epidemiological studies suggest that daily intake of fruits and vegetables high in polyphenols or the addition of olive oil containing many polyphenols is associated with a reduced risk of chronic diseases including cardiovascular, metabolic, neurodegenerative, and inflammatory bowel conditions. In vivo experiments demonstrated that the administration of a diet associated with daily intake of extra virgin olive oil (EVOO) reduces histological lesions and symptomatology in rats with a dextran sulfate sodium (DDS) induced colitis. A diet supplemented with hydroxytyrosol (a component of olive oil) showed a reduction of the inflammatory process at the inflamed colon of the rats.
Detailed Description
Ulcerative colitis (UC) is a chronic inflammatory bowel disease of unknown etiology, which usually occurs in young adults (II-IV decade of life). Epidemiological data have shown a north-south gradient of both incidence and prevalence of UC in European countries, with a higher prevalence in northern European countries than in the Mediterranean area. However, recent data show a reduction in these differences in the last two decades. The reasons of this reduction are unknown, but it is possible that these differences are related to a change in dietary habits in southern European countries where a diet rich in fresh fruits and vegetables (the so-called "Mediterranean diet") is gradually being replaced by a typical diet of the industrialized countries of northern Europe, characterized by high consumption of frozen or pre-packaged foods of the food industry. These changes in the diet regime have also replaced the type of oil contained in foods, ranging from olive oil (typical of the Mediterranean diet) to fats of animal origin or vegetable oils not coming from the olives. Olive oil is universally recognized as the symbol of the Mediterranean diet and its beneficial properties have been extensively studied. In particular, there are scientific evidence showing an effect of virgin olive oil on the lipid metabolism, on chronic inflammation, on blood pressure, and the regulation and detoxification of free radicals. In particular, beneficial effects would in part be related to polyphenols, potent natural antioxidants contained in olive oil. Monocultivar Coratina extra virgin olive oil (MC-EVOO) is an Apulian olive oil that, while possessing an extraordinary health effect superior to other cultivars, is not very used because of its distinctive characteristics of bitter and spicy. The bitter and the spicy of the extra virgin olive oil obtained from Coratina monocultivar are not defects in the oil but are the expression of a very high concentration of polyphenols (up to 800-1000 mg / kg of oil) compared to other varieties which, as well as providing extraordinary health benefits to the consumer, extend the expiration date of the oil itself, preserving it from oxidative action. The MC-EVOO is a typical of the Apulia Region and it is characterized by: high content of polyphenols natural 100% product, with no residues of chemical solvents and other toxic and harmful contaminants. No studies have been published so far that have demonstrated a potential toxic effects of polyphenols. Instead, EVOO-C supplementation could potentially have positive effects on lipid metabolism and body weight. Epidemiological studies suggest that daily intake of fruits and vegetables high in polyphenols or the addition of olive oil containing many polyphenols is associated with a reduced risk of chronic diseases including cardiovascular, inflammatory, metabolic, neurodegenerative, and some neoplasms. Also the results of in vitro study showed these properties but these results have to be carefully evaluated because in vivo the polyphenols, after being absorbed into the intestine and conjugated in the liver, arrive in the blood in methylated, sulphated and glycogenated form. These molecules are completely different from the structural point of view of native molecules. Moreover, their presence is in the concentration of nano or micro molecules. These molecules have different biological properties from native ones and are distributed differently in different tissues and cells. In addition, in the in-vitro studies native polyphenol molecules have been used at high concentrations, or above physiological (over 100 micromoles). This is the first reason why a clinical trial case study was planned. Polyphenols also modulate cell membranes, enzymes, transcription factors and receptors. This is the second reason why nutrigenomics will be studied during the course of the clinical trial to evaluate the effects of polyphenols on the molecular and cellular mechanisms of the inflammatory processes that are present in the ulcerative colitis. In vivo experiments demonstrated that the administration of a diet associated with daily intake of EVOO reduces histological lesions and symptomatology in rats with a DDS induced colitis. A diet supplemented with hydroxytyrosol (a component of olive oil) showed a reduction of the inflammatory process at the inflamed colon of the rats. These data show that EVOO supplementation in a diet can improve the course of the disease. Experimental studies in humans are limited. The first study published over 25 years ago concluded that administering a supplement of fish oil to the diet produced a modest reduction in corticosteroid in the active phases of the disease, but not a benefit in maintenance therapy over olive oil. This work presents important limitations: the content of polyphenols in the oils used is unknown the remission time between the two oils was not statistically significant there are no data on inflammation of the colon before and after treatment Recently, an in vitro study performed on intestinal mucosa obtained from 14 active UC patients showed that samples treated with oleuropein had a reduced expression of two inflammatory factors, COX-2 and IL-17, suggesting that olive oil containing oleuropein can improve inflammatory status. The aim of the study is to evaluate whether MC- EVOO supplementation in moderate to severe UC patients needing a steroid cycle may increase the clinical response rate to medical therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis Chronic Mild
Keywords
Ulcerative colitis, UC, Extra virgin olive oil, Polyphenols

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Pilot study
Masking
ParticipantInvestigator
Masking Description
Patients will receive a bottle with experiental oil or placebo, consisting of commercial refined olive oil. No diffencences between the two bottles.
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MC-EVOO in addition to steroid therapy
Arm Type
Active Comparator
Arm Description
Oral beclomethasone dipropionate at dose of 10 mg / day for the first 4 weeks, 5 mg / day for the second 4 weeks plus MC- EVOO for 12 weeks at a dose of 2 tablespoons per day (1 before lunch and 1 before dinner). Each spoon will contain 10 grams of oil containing 5 mg of biophenols.
Arm Title
Refined olive oil and steroid therapy
Arm Type
Placebo Comparator
Arm Description
Oral beclomethasone dipropionate (10 mg / day for the first 4 weeks, 5 mg / day for the second 4 weeks) plus placebo consisting of refined olive oil with low biophenols.
Intervention Type
Combination Product
Intervention Name(s)
Beclomethasone dipropionate in addition to MC-EVOO
Intervention Description
Oral beclomethasone dipropionate at dose of 10 mg / day for the first 4 weeks, 5 mg / day for the second 4 weeks plus MC- EVOO for 12 weeks at a dose of 2 tablespoons per day (1 before lunch and 1 before dinner). Each spoon will contain 10 grams of oil containing 5 mg of biophenols.
Intervention Type
Combination Product
Intervention Name(s)
Beclomethasone dipropionate in addition to refined oil
Intervention Description
Oral beclomethasone dipropionate (10 mg / day for the first 4 weeks, 5 mg / day for the second 4 weeks) plus placebo consisting of refined olive oil with low biophenols.
Primary Outcome Measure Information:
Title
Evaluation of the short-term clinical response
Description
Evaluation of the short-term clinical response rate in the 2 treatment groups
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Evaluation of the clinical remission
Description
Evaluation of the clinical remission rate in the short term in the 2 treatment groups
Time Frame
12 weeks
Title
Evaluation of the endoscopic remission
Description
Evaluation of the endoscopic remission rate after 3 months in the 2 treatment groups
Time Frame
12 weeks
Title
Evaluation of markers of inflammation
Description
Evaluation of the rate of patients with normalization of markers of inflammation in the short and medium term in the 2 treatment groups
Time Frame
12 weeks
Title
Evaluation of adverse events
Description
Evaluation of the rate of adverse events in the 2 treatment groups
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with active UC (diagnosed for at least 3 months) aged 18 to 70 years Patients with mild to moderate disease (calculated by Mayo score). Patients can provide their informed consent to participate in the study Exclusion Criteria: Patients with Crohn's disease Patients with complicated disease, who are candidates for urgent surgery Patients with colostomy Patients with contraindications to steroid therapy (diabetes mellitus, severe osteoporosis, vertebral fractures, previous intolerance to steroid therapy) Patients with unstable or inappropriately controlled cardiovascular, pulmonary, hepatic, renal or hematologic diseases Patients who are not compliant Patients abusing alcohol or drugs
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fabrizio Bossa, MD
Phone
+39 0882416281
Email
f.bossa@operapadrepio.it
Facility Information:
Facility Name
IRCCS Casa Sollievo della Sofferenza
City
San Giovanni Rotondo
State/Province
Foggia
ZIP/Postal Code
71013
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Angelo Andriulli, MD
Phone
0039 0882 410263
Email
a.andriulli@operapadrepio.it
First Name & Middle Initial & Last Name & Degree
Orazio Palmieri, BSc
Phone
0039 0882416281
Email
o.palmieri@operapadrepio.it

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22047562
Citation
Danese S, Fiocchi C. Ulcerative colitis. N Engl J Med. 2011 Nov 3;365(18):1713-25. doi: 10.1056/NEJMra1102942. No abstract available.
Results Reference
background
PubMed Identifier
23335431
Citation
Ng SC, Bernstein CN, Vatn MH, Lakatos PL, Loftus EV Jr, Tysk C, O'Morain C, Moum B, Colombel JF; Epidemiology and Natural History Task Force of the International Organization of Inflammatory Bowel Disease (IOIBD). Geographical variability and environmental risk factors in inflammatory bowel disease. Gut. 2013 Apr;62(4):630-49. doi: 10.1136/gutjnl-2012-303661. Epub 2013 Jan 18.
Results Reference
background
PubMed Identifier
18186549
Citation
Koloski NA, Bret L, Radford-Smith G. Hygiene hypothesis in inflammatory bowel disease: a critical review of the literature. World J Gastroenterol. 2008 Jan 14;14(2):165-73. doi: 10.3748/wjg.14.165.
Results Reference
background
PubMed Identifier
21874330
Citation
Sanchez-Fidalgo S, Sanchez de Ibarguen L, Cardeno A, Alarcon de la Lastra C. Influence of extra virgin olive oil diet enriched with hydroxytyrosol in a chronic DSS colitis model. Eur J Nutr. 2012 Jun;51(4):497-506. doi: 10.1007/s00394-011-0235-y. Epub 2011 Aug 27.
Results Reference
background
PubMed Identifier
24445043
Citation
Takashima T, Sakata Y, Iwakiri R, Shiraishi R, Oda Y, Inoue N, Nakayama A, Toda S, Fujimoto K. Feeding with olive oil attenuates inflammation in dextran sulfate sodium-induced colitis in rat. J Nutr Biochem. 2014 Feb;25(2):186-92. doi: 10.1016/j.jnutbio.2013.10.005. Epub 2013 Nov 8.
Results Reference
background
PubMed Identifier
27016717
Citation
Reddy KVK, Naidu KA. Oleic acid, hydroxytyrosol and n-3 fatty acids collectively modulate colitis through reduction of oxidative stress and IL-8 synthesis; in vitro and in vivo studies. Int Immunopharmacol. 2016 Jun;35:29-42. doi: 10.1016/j.intimp.2016.03.019. Epub 2016 Mar 24.
Results Reference
background
PubMed Identifier
1353742
Citation
Hawthorne AB, Daneshmend TK, Hawkey CJ, Belluzzi A, Everitt SJ, Holmes GK, Malkinson C, Shaheen MZ, Willars JE. Treatment of ulcerative colitis with fish oil supplementation: a prospective 12 month randomised controlled trial. Gut. 1992 Jul;33(7):922-8. doi: 10.1136/gut.33.7.922.
Results Reference
background
PubMed Identifier
28420140
Citation
Larussa T, Oliverio M, Suraci E, Greco M, Placida R, Gervasi S, Marasco R, Imeneo M, Paolino D, Tucci L, Gulletta E, Fresta M, Procopio A, Luzza F. Oleuropein Decreases Cyclooxygenase-2 and Interleukin-17 Expression and Attenuates Inflammatory Damage in Colonic Samples from Ulcerative Colitis Patients. Nutrients. 2017 Apr 15;9(4):391. doi: 10.3390/nu9040391.
Results Reference
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Monocultivar Coratina Extra Virgin Olive Oil in UC Patients

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