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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00395954
Other study ID # UHL 10217
Secondary ID
Status Completed
Phase Phase 0
First received November 2, 2006
Last updated February 13, 2009
Start date November 2006
Est. completion date June 2007

Study information

Verified date February 2009
Source University Hospitals, Leicester
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Observational

Clinical Trial Summary

The hypothesis underlying this study is that failure to recognise the role of lactose intolerance among patients has led to inappropriate dietary advice and treatment with drugs that contain lactose as a filler. These failures exacerbate symptoms and lead to the unnecessary use of immune suppressant drugs.

This study will identify the threshold at which symptoms of lactose intolerance develop, to provide appropriate advice and treatment in the management of patients.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date June 2007
Est. primary completion date June 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Confirmed lactose intolerance demonstrated with a lactose intolerance test.

- Adherence to a lactose free diet for at least four days before the start of the study.

Exclusion Criteria:

- Failure to adhere to a lactose free diet.

- People who are on lactose containing medications.

- Pregnancy.

- Unwillingness to comply with study outline.

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospitals, Leicester
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