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Vasodilation Effect of Inhalational Anesthetics

Vasodilation Effect of Inhalational Anesthetics Including Halothane, Isoflurane, Sevoflurane, Desflurane and Enflurane

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00815269
Acronym
VEFIHA
Enrollment
300
Registered
2008-12-29
Start date
2008-12-31
Completion date
2009-12-31
Last updated
2009-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

General Anesthesia

Keywords

Inhalant anesthetic, Vasodilation, General anesthesia, Ultrasonography

Brief summary

Previous studies on animals suggest that inhalational anesthetics can reduce vascular tension in vitro resulting in vasodilation and decrease in blood pressure. This role for inhalational anesthetics has essential clinical implications such as the condition of sepsis or septic shock or other shock-associated states during which the blood vessel constricts strongly and leads to circulation dysfunction. The vasodilation property of these anesthetics including halothane, isoflurane, sevoflurane, desflurane and enflurane enables them to be better options than other general anesthetics in many clinical conditions needing the vasculature to be dilated. The investigators hypothesized that these inhalational anesthetics can evoke vasodilation measured with ultrasonography during general anesthesia in vivo as the in vitro studies displayed.

Interventions

DRUGHalothane

Induction: 2-4% halothane pluses 3-5 L/min oxygen Maintenance: different doses from 0.5% to 3% with 1-2 L/min oxygen

DRUGIsoflurane

Induction: 2-5% isoflurane pluses 3-5 L/min oxygen Maintenance: different doses from 1% to 4% with 1-2 L/min oxygen

DRUGSevoflurane

Induction: 3-8% sevoflurane pluses 3-5 L/min oxygen Maintenance: different doses from 1% to 4% with 1-2 L/min oxygen

DRUGDesflurane

Induction: 2-8% desflurane pluses 3-5 L/min oxygen Maintenance: different doses from 1% to 4% with 1-2 L/min oxygen

DRUGEnflurane

Induction: 2-5% enflurane pluses 3-5 L/min oxygen Maintenance: different doses from 1% to 4% with 1-2 L/min oxygen

Sponsors

Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Must be undergoing general anesthesia * Age between 19-45 years

Exclusion criteria

* With hypertension * Existing organic dysfunction * Allergic to inhalant anesthetics * Alcohol addictive or narcotic dependent patients * A history of the use of centrally-acting drugs of any sort, chronic pain and psychiatric diseases records

Design outcomes

Primary

MeasureTime frame
Ultrasonography of blood vessels including radial artery, brachial artery, femoral artery, popliteal arteryTen min prior to anesthesia; 0 min of anesthesia; 0 min of the end of anesthesia induction; 5, 10, 20, 30, 60 min during maintenance of the anesthesia

Secondary

MeasureTime frame
Blood flow volume during anesthesia of the vasculatureTen min prior to anesthesia; 0 min of anesthesia; 0 min of the end of anesthesia induction; 5, 10, 20, 30, 60 min during maintenance of the anesthesia
Blood pressure including systolic, diastolic and mean artery blood pressuresTen min prior to anesthesia; 0 min of anesthesia; 0 min of the end of anesthesia induction; 5, 10, 20, 30, 60 min during maintenance of the anesthesia
The time interval of between the initiation of the inhalational anesthetics delivered to the beginning of decreasing of blood pressureFrom the beginning of anesthesia (0 min) till the first time of blood pressure decreased, this measure would be varied according to different individuals
The total dose of phenylephrine required to maintain baseline arterial blood pressureFrom the beginning of anesthesia (0 min) to 20 min after anesthesia begun
Regression and correlation analyses between different doses of the anesthetics and the extent of vasodilationForty eight hours after operation

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026