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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06124027
Other study ID # MEC-2022-0421
Secondary ID NL81086.078.22
Status Recruiting
Phase
First received
Last updated
Start date February 13, 2023
Est. completion date November 30, 2023

Study information

Verified date November 2023
Source Erasmus Medical Center
Contact Calvin de Wijs, MSc
Phone 0107032804
Email c.dewijs@erasmusmc.nl
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Deep procedural sedation has seen an increased use indication over the last couple of years aided by the introduction of high flow nasal oxygen therapy (HFNOT) during these procedures. However, this level of deep sedation does come with the increased risk of examining whether a patient is adequately ventilated during this procedure. The definition of deep sedation is: 'a drug-induced depression of consciousness during which patients cannot be easily aroused but respond purposefully following repeated or painful stimulation. The ability to independently maintain ventilatory function may be impaired. Patients may require assistance in maintaining a patent airway, and spontaneous ventilation may be inadequate. Cardiovascular function is usually maintained.' As the definition showed there may be an insufficient ventilation during deep sedation. Therefore, HFNOT is used to ensures that the peripheral oxygen saturation is sufficient. However, there are two potential disadvantages. HFNOT can mask the presence of an insufficient respiratory minute volume and an insufficient gas exchange, which can lead to high arterial CO2 (paCO2) levels. Another risk associated with HFNOT is the fact that high oxygen levels are toxic, and prolonged exposure to high partial oxygen pressures, can cause oxidative damage to cell membranes, collapse of the alveoli in the lungs, retinal detachment, and seizures. Most of this damage can be explained by hyperoxia that increases the 'leak' of electrons from the mitochondrial electron transport chain and the resulting increased generation of reactive oxygen species (ROS). Low paCO2 levels and hyperoxia cannot be examined using standard monitoring techniques therefore, this study will use the transcutaneous carbon dioxide (tcPCO2) a proven technique which correlates well to the arterial CO2 (paCO2) to evaluate whether there is an adequate level of ventilation during deep procedural anesthesia with HFNOT. Moreover, the cutaneous mitochondrial oxygenation (mitoPO2) will be monitored to determine the effects that deep procedural sedation with HFNOT has on the cellular oxygenation.


Recruitment information / eligibility

Status Recruiting
Enrollment 35
Est. completion date November 30, 2023
Est. primary completion date November 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age over 18 years - Acceptable proficiency of the Dutch language - Scheduled for a procedure requiring deep procedural sedation with HFNOT. Exclusion Criteria: - Porphyria - Known intolerance to components of the ALA plaster - Presence of mitochondrial disease - Pregnancy/lactation - Patients with skin lesions on the measurement location which impede measurements - Incapability to provide inform consent, due to a mental condition interfering with the ability to understand the provided information

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Monitoring tcPCO2 and mitoPO2
Monitoring tcPCO2 using SenTec and mitoPO2 using COMET

Locations

Country Name City State
Netherlands Erasmus MC Rotterdam South Holland

Sponsors (1)

Lead Sponsor Collaborator
Calvin de Wijs, MSc

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary tcPCO2. To examine the effects of deep procedural sedation and use of HFNOT on the tcPCO2. up to 6 hours
Primary mitoPO2 To determine the effects of deep procedural sedation and use of HFNOT on the mitoPO2 up to 6 hours
Secondary mitoVO2 To determine the effects of deep procedural sedation and use of HFNOT on the mitoVO2 up to 6 hours
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