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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02423460
Other study ID # 1000046356
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2015
Est. completion date September 23, 2018

Study information

Verified date November 2018
Source Nestlé
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The daily requirement of threonine, an essential amino acid, will be evaluated in healthy adult males and in adult males with Crohn's Disease or ulcerative colitis using the indicator amino acid oxidation (IAAO) method. Participants will consume specially formulated diets with varying levels of threonine.


Description:

Threonine is an essential amino acid which must be obtained from the diet. It is a component of mucin. Mucin, in turn, is a key protein in the mucous membrane that protects the lining of the intestine.

Inflammatory bowel disease (IBD) is a group of inflammatory conditions that affect the colon and small intestine. IBD primarily includes ulcerative colitis (UC) and Crohn's disease (CD). In UC, the inflammation is usually in the colon whereas in CD inflammation may occur anywhere along the digestive tract. Studies in animals have shown that more threonine is used when there is inflammation in the intestine.

The threonine requirement in healthy participants and in IBD patients will be determined using the indicator amino acid oxidation method. The requirement derived in healthy participants will be compared to that derived in patients with IBD.

Each participant will take part in two x 3 day study periods. The first two days are called adaptation days where the subjects will consume a liquid diet specially designed for him. The diet will be consumed at home. It contains all vitamins, minerals, protein and all other nutrients required. On the third day, the participant will come to the Hospital for Sick Children in Toronto. Subjects will consume hourly meals for a total of 8 meals and a stable isotope 13C-phenylalanine. Breath and urine samples will be collected to measure the oxidation of phenylalanine from which the threonine requirement will be determined.


Recruitment information / eligibility

Status Completed
Enrollment 86
Est. completion date September 23, 2018
Est. primary completion date September 17, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria (healthy controls):

- Male age 18 - 40 years of age

- Having obtained his (or his legal representative's) written informed consent.

- Normally nourished and without any inter-current illness.

- Absence of an active inflammatory process in the past month.

Exclusion Criteria (healthy controls):

- Subject who cannot be expected to comply with the study procedures.

- Currently participating or having participated in another clinical study during the last 4 weeks prior to the beginning of this study.

Inclusion Criteria: Crohn's Disease and Ulcerative Colitis

- Male age 18 - 40 years of age

- Having obtained his (or his legal representative's) Written Informed Consent.

- For both conditions, stable disease state and not malnourished per the treating physician.

- CD: Harvey Bradshaw Index (HBI) = 8, disease location: evidence of ileal and or colon inflammatory involvement, no known strictures

- UC: Mayo Score = 7 (or Partial Mayo Score =5)

- No tube feeding - Subjects must be treated and followed by the Gastroenterology team at Mt. Sinai Hospital, Toronto.

Exclusion Criteria: Crohn's Disease and Ulcerative Colitis

- Uncontrolled inflammation which will likely require surgery or escalation of therapy in the next 4 weeks

- Concomitant treatment:corticosteroids > 20mg/day

- Subject who cannot be expected to comply with the study procedures. - Subjects not treated and followed by the Gastroenterology team at Mt. Sinai Hospital, Toronto

Study Design


Intervention

Other:
Threonine
Threonine will be fed at various intake levels ranging from high to low in order to determine its requirement in healthy males and in patients with Crohn's disease and Ulcerative colitis.

Locations

Country Name City State
Canada The Hospital for Sick Children Toronto Ontario

Sponsors (3)

Lead Sponsor Collaborator
Nestlé Mount Sinai Hospital, Canada, The Hospital for Sick Children

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Threonine requirement in those with Crohn's Disease, ulcerative colitis and in healthy controls determined using the indicator amino acid oxidation method 2 years
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