The Effect of Phenylephrine and Ephedrine on Microvascular Blood Flow
Information source: University of Nottingham
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Healthy Volunteers
Intervention: Administration of phenylephrine (Drug); Measurement of stroke volume (Other); Contrast enhanced ultrasound scan (Other); Administration of ephedrine (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: University of Nottingham Official(s) and/or principal investigator(s): John P Williams, PhD, Principal Investigator, Affiliation: University of Nottingham
Overall contact: John P Williams, PhD, Email: john.williams7@nhs.net
Summary
During operations to treat abdominal problems the blood pressure can fall, resulting in
falls in blood flow to the vital organs. This fall can be treated by the administration of
drugs that cause constriction of blood vessels. Although these drugs correct falls in blood
pressure, it is unclear what effect they have on blood flow from the heart and to the vital
organs.
In this study of healthy volunteers we aim to better understand the changes in blood flow in
both small and large vessels that occur in response to administration of these drugs. To do
this we will use two different techniques of ultrasound imaging. A narrow (4-5mm) ultrasound
probe will be inserted into the oesophagus via a nostril to measure blood flow in a major
blood vessel. A second probe will rest on the abdomen and will record changes in blood flow
in small vessels of the liver. Two drugs which raise the blood pressure via different
mechanisms will be administered and the changes in flow from the heart and to vital organs
will be measured and compared.
Clinical Details
Official title: An Observational Study to Test the Effect of the Vasoactive Drugs Phenylephrine and Ephedrine on the Stroke Volume and Microvascular Blood Flow of Healthy Volunteers
Study design: Time Perspective: Prospective
Primary outcome: Change in microvascular blood flow
Secondary outcome: Change in stroke volume
Detailed description:
Optimising the cardiac output is essential to ensure adequate organ perfusion in patients
who are undergoing major surgery. To enable this cardiac output (CO) is frequently monitored
during operations using a variety of techniques; one such technique is trans-oesophageal
Doppler ultrasound also known as oesophageal Doppler monitoring (ODM). ODM measurement of CO
is a less invasive technique than many currently used methods, and has recently been
recommended by NICE for adoption in clinical practice. The matching of microvascular blood
flow and CO is advantageous for visceral organs, in marrying demands for oxygen and
nutrients to their delivery. Major surgery and the attendant requirement for general
anaesthesia can result in dramatic changes in blood pressure (BP) and CO. These changes can
be corrected by the administration of vasoactive drugs such as phenylephrine and ephedrine,
although it is unclear what effects these drugs have on microvascular blood flow (MVBF) to
the intra-abdominal viscera. Whilst they correct falls in BP, and hence may increase
visceral flow, this increased BP is partially mediated via splanchnic vasoconstriction,
which may result in decreased blood flow. A greater appreciation of the effect of these
vasoactive drugs on the CO and MVBF may help with the development of more refined algorithms
for their use in the clinical setting. In our clinical physiology laboratories we regularly
employ contrast-enhanced ultrasound (CEUS) using a Phillips iU22, to measure MVBF in healthy
males following a variety of physiological challenges. This minimally invasive ultrasound
based imaging technique is ideal for gaining an insight into the effect various
physiological interventions have on tissue blood flow and could be readily used to chart
changes in visceral MVBF and CO following vasoactive drug administration. Transference of
this investigative approach to a clinical setting has the potential to greatly improve the
care of the surgical patient under anaesthesia.
Eligibility
Minimum age: 18 Years.
Maximum age: 60 Years.
Gender(s): Male.
Criteria:
Inclusion Criteria:
- Aged 18-60 years
- Male
- Able to consent in English by themselves
- Absence of any exclusion criteria
Exclusion Criteria:
- A BMI < 20 or > 28 kg•m2
- Active cardiovascular disease: uncontrolled hypertension (BP > 140/90), angina, heart
failure (class III/IV), arthymia, right to left cardiac shunt or recent cardiac event
- Individuals taking alpha or beta-adrenergic blocking agents, monoamine oxidase
inhibitors, tricyclic antidepressants, serotonin or noradrenaline selective reuptake
inhibitors, quinidine, cardiac glycosides or buspirone (or who have ceased taking
them in the previous 14 days¬)
- Cerebrovascular disease: previous stroke, aneurysm (large vessel or intracranial)
- Peripheral vascular disease
- 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
- Known prostatic hypertrophy
- 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, ephedrine or phenylephrine
- Participants who have taken part in any other research study in the last three months
which involved: taking a drug; being paid a disturbance allowance; having an invasive
procedure (eg blood sample >50ml, muscle biopsies) or exposure to ionising radiation.
Locations and Contacts
John P Williams, PhD, Email: john.williams7@nhs.net
University of Nottingham, School of Medicine, Division of Medical Sciences and Graduate Entry Medicine, Derby, Derbyshire DE22 3DT, United Kingdom; Recruiting David Read, BMBS, Email: dread1@nhs.net John P Williams, PhD, Principal Investigator Thomas P Heinink, BMBS, Sub-Investigator Jonathan N Lund, MD, Sub-Investigator Bethan E Phillips, PhD, Sub-Investigator David Read, BMBS, Sub-Investigator
Additional Information
Starting date: August 2014
Last updated: January 26, 2015
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