Study Results
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Basic Information
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COMPLETED
PHASE4
15 participants
INTERVENTIONAL
2009-07-31
2009-11-30
Brief Summary
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Detailed Description
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Interested participants will be asked to attend a screening interview during which the study procedures/risks/benefits will be explained, followed by a brief history and physical examination. If deemed necessary by the study investigator, a 7ml sample of blood will be taken for screening purposes. The volunteer will be deemed eligible for the study once they have passed the screening visit and \[when performed\] had normal screening blood investigation results.
Each volunteer will be studied 3 times, the order of which will be determined randomly by computer. Participants will report for the study at the Division of GI Surgery (E-floor, West Block, Queen's Medical Centre), at 7:15am. On arrival the subject's height and weight will be recorded and 'drip needle' will will be placed in the back of the wrist. The hand will be rested in a hand-heater allowing venous blood to be sampled.
The subject will be randomly allocated to receive one of the three study drinks. At 7:50am baseline blood will be sampled (10ml \[1.5 tablespoons\] via the drip needle). At 8am the volunteers will drink the study drink. The rate of stomach emptying will be measured by using Gamma scintigraphy (a specialised medical camera). The drinks will have added a tracer substance that is visible on the camera and allows us to follow drink as it passes through the stomach into the bowels. Each 'picture' of the stomach lasts 20 seconds and we plan to take these every 20 minutes for 4 hours after intake of the drink. At 20 minute intervals (until 220 mins have elapsed) 7ml (1 tablespoon) of blood will be sampled via the drip needle. The final 10 ml blood sample will be taken at 240 minutes following which the drip needle will be removed and the volunteers will be allowed home. The subsequent two studies will be performed 7 days following the first study.
In total 95ml (a sixth of a pint) blood will be taken during each of the 3 crossover studies which will be separated by a period of 7 days (i.e. a total of 285 ml \[half a pint\] blood will be required from each volunteer).
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
SINGLE
Study Groups
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Nutricia PreOp + Lipid
Nutricia PreOp + Lipid
Nutricia PreOp nutritional supplement
nutritional supplement
Lipid
Drink
Nutrica PreOP + Glutamine
Nutrica PreOP + Glutamine
Nutricia PreOp nutritional supplement
nutritional supplement
Glutamine
Drink
Nutricia PreOP
Nutricia PreOP: carbohydrate only drink
Nutricia PreOp nutritional supplement
nutritional supplement
Interventions
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Nutricia PreOp nutritional supplement
nutritional supplement
Lipid
Drink
Glutamine
Drink
Eligibility Criteria
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Inclusion Criteria
* BMI of 20-25 kg/m2,
* Able to give voluntary written informed consent to participate in the study,
* Able to understand the requirements of the study, including anonymous publication, and agree to co-operate with the study procedures.
Exclusion Criteria
* Smoking,
* Regular medication or substance abuse,
* Have taken part in any other clinical study within the previous 3 months.
18 Years
60 Years
MALE
Yes
Sponsors
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University of Nottingham
OTHER
Responsible Party
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University of Nottingham
Principal Investigators
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Dileep N Lobo, FRCS
Role: PRINCIPAL_INVESTIGATOR
University of Nottingham
Locations
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Nottingham Digestive Diseases Centre Biomedical Research Unit
Nottingham, Nottinghamshire, United Kingdom
Countries
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References
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Awad S, Constantin-Teodosiu D, Macdonald IA, Lobo DN. Short-term starvation and mitochondrial dysfunction - a possible mechanism leading to postoperative insulin resistance. Clin Nutr. 2009 Oct;28(5):497-509. doi: 10.1016/j.clnu.2009.04.014. Epub 2009 May 17.
Awad S, Blackshaw PE, Wright JW, Macdonald IA, Perkins AC, Lobo DN. A randomized crossover study of the effects of glutamine and lipid on the gastric emptying time of a preoperative carbohydrate drink. Clin Nutr. 2011 Apr;30(2):165-71. doi: 10.1016/j.clnu.2010.09.008. Epub 2010 Oct 23.
Other Identifiers
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09026
Identifier Type: -
Identifier Source: org_study_id
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