Healthy Volunteers Clinical Trial
Official title:
Investigation of the Relationship Between Oesophageal Doppler Assessed Increases in Cardiac Output and Microvascular Visceral Blood Flow in Healthy Volunteers
| Verified date | January 2015 |
| Source | University of Nottingham |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United Kingdom: Research Councils UK |
| Study type | Observational |
Although major surgery is often required to treat abdominal problems, there is a significant
risk of death or complication following these operations. By using ultrasound the amount and
timing of fluid patients receive during operations can be optimised and the risk of surgery
reduced. However, little is known about the exact changes in blood flow in the small vessels
of the body in response to fluid. A greater understanding of this may allow for more
appropriate care of patients undergoing this type of surgery in the future.
In this study of healthy volunteers we will attempt to better understand how fluid
administration guided by ultrasound effects blood flow in large and small vessels, by using
two different techniques of ultrasound imaging. A narrow bore (approximately 4-5mm diameter)
ultrasound probe will be passed through the nostril and mouth to rest within the oesophagus
allowing measurement of blood flow in the main artery, while a second probe will be rested
on the volunteer's abdomen and used to record changes in blood flow in small liver blood
vessels. Comparison of these two techniques during the administration of fluid will allow us
to better understand the relationship between large and small vessel blood flow.
Because different types of fluid may behave in different ways, we will test the effect of
two types of fluid commonly used in clinical practice; `normal` saline solution and
gelofusine.
| Status | Completed |
| Enrollment | 24 |
| Est. completion date | August 2014 |
| Est. primary completion date | March 2014 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Male |
| Age group | 18 Years to 80 Years |
| Eligibility |
Inclusion Criteria: - male - age 18-80 years - body mass index 20-30kg/m2 Exclusion Criteria: - BMI < 20 or > 30 kg/m2. - Active cardiovascular disease: uncontrolled hypertension (BP > 160/100), angina, heart failure (class III/IV), arhythmias , right to left cardiac shunt or recent cardiac event. - Individuals taking beta-adrenergic blocking agents. - Cerebrovascular disease: previous stroke, aneurysm (large vessel or intracranial).. - Metabolic disease: hyper and hypo parathyroidism, untreated hyper and hypothyroidism, Cushing's disease, types 1 or 2 diabetes. - Active inflammatory bowel disease, or renal disease, - Malignancy - Clotting dysfunction - Previous oesophageal surgery - Individuals with a known history of oesophageal varices - Individuals with a known history of epistaxis - Family history of early (<55y) death from cardiovascular disease. - Known sensitivity to SonoVue - Known sensitivity to gelofusine |
Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | University of Nottingham, School of Medicine, Division of Medical Sciences and Graduate Entry Medicine | Derby | Derbyshire |
| Lead Sponsor | Collaborator |
|---|---|
| University of Nottingham |
United Kingdom,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in microvascular visceral blood flow | Microvascular visceral blood flow is assessed using contrast enhanced ultrasound scanning, following stroke volume optimisation. | 30 minutes | No |
| Secondary | Change in stroke volume | The change in stroke volume will be assessed using an Oesophageal Doppler Monitor, and will be assessed pre- and post-intravenous fluid administration. | 30 minutes | No |
| Secondary | Change in haematocrit | The change in the haematocrit will be measured pre- and post-intravenous fluid administration. | 60 minutes | No |
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