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Cerebral Oxygenation Values in Healthy Adults Volunteers Measured With RheoPatch and NIRO-200NX

Comparison of Cerebral Oxygenation Values in Healthy Adults

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05460585
Enrollment
28
Registered
2022-07-15
Start date
2022-06-01
Completion date
2023-05-10
Last updated
2023-05-15

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

Conditions

Adults, Healthy

Brief summary

Noninvasive measurement of cerebral tissue oxygen saturation levels by near infrared spectroscopy (NIRS) is clinical routine in perioperative medicine. One of the main technical challenges of NIRS measurements is to eliminate the influence of signals of the skin and skull. A new device (RheoPatch, Luciole Medical AG, Zurich) has been developed by a company that also developed an intracranial NIRS probe, which allowed measurements directly in the brain and thus improved algorithms for elimination of the extracranial signals. The investigators aim to determine baseline values and performance of the new device (RheoPatch) compared with a more established NIRS device (NIRO-200NX, Hamamatsu Phototonics, Hamamatsu City, Japan)

Detailed description

Primary objective is to compare the RheoPatch NIRS device with the NIRO-200NX NIRS device in volunteers at rest in supine position. As secondary objectives, repeatability of the measurements will be tested with optode reapplications. With measurements in Trendelenburg position, the investigators evaluate the influence of body (head) position on the NIRS signals. Primary outcome are the baseline values of cerebral oxygenation levels measured by RheoPatch (SbtO2 (%)) and NIRO-200NX (Tissue oxygenation index: TOI (%)). Secondary endpoints are the repeatability of the measurements with sensor reapplications (coefficient of repeatability, 5 repeats with each device) and changes of the measurements of cerebral oxygenation saturation level in the Trendelenburg position. Measurements of baseline cerebral oxygenation values are obtained in supine position with 10 measurements, alternating between devices. Combined with 5 min measurement phase for equilibration and power adjustment, this will require 33 minutes per participant.

Interventions

DEVICECerebral oximetry using Rheopatch

On the study visit, baseline demographic data (age and gender, BMI) are collected. In supine position the sensor patches (left and right) of the device are applied to the forehead and the cerebral oxymetry values are recorded during 120sec. The sensor patches are then removed and the patches of the second device are applied on the same position on the forehead and the measurement is carried out as described before. For the first measurement of each sensor, a total of 5 minutes equilibration and sensor output power adjustment is allowed. A total of 10 measurements are taken, 5 with each device. The volunteer is then placed in Trendelenburg position and another 4 measurements are made (2 with each device) as previously described.

DEVICECerebral oximetry using NIRO-200NX

On the study visit, baseline demographic data (age and gender, BMI) are collected. In supine position the sensor patches (left and right) of the device are applied to the forehead and the cerebral oxymetry values are recorded during 120sec. The sensor patches are then removed and the patches of the second device are applied on the same position on the forehead and the measurement is carried out as described before. For the first measurement of each sensor, a total of 5 minutes equilibration and sensor output power adjustment is allowed. A total of 10 measurements are taken, 5 with each device. The volunteer is then placed in Trendelenburg position and another 4 measurements are made (2 with each device) as previously described.

Sponsors

Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

Subjects fulfilling all of the following inclusion criteria are eligible for the investigation: * Informed Consent signed by the subject * Subjective good health

Exclusion criteria

The presence of any one of the following

Design outcomes

Primary

MeasureTime frameDescription
Cerebral oxygen saturation levelOne dayPrimary endpoint is the cerebral oxygen saturation level measured by RheoPatch (SbtO2 (%)) and NIRO-200NX (Tissue oxygenation index: TOI (%)). This is the value used for clinical decision making in the daily routine when NIRS measurement devices are used in perioperative medicine or intensive care applications and therefore the most relevant value.

Secondary

MeasureTime frameDescription
nTHI_NIROOne dayNormalized tissue hemoglobin index: nTHI (absolute value in arbitrary unit)
ΔO2Hb_NIROOne dayOxygenated hemoglobin change: ΔO2Hb (μmol/L)
ΔHHb_NIROOne dayDeoxygenated hemoglobin change: ΔHHb (μmol/L)
ΔcHb_NIROOne dayTotal hemoglobin change: ΔcHb (μmol/L)
aH2O_RPOne dayAbsolute concentration of brain tissue water: aH2O (mmol/L)
Changes of the measurements of cerebral oxygenation saturation level (SbtO2 (%) and TOI (%))One daySbtO2 and TOI changes are measured
aHbOxy_RPOne dayAbsolute concentration of oxygenated hemoglobin: aHbOxy (μmol/L)
aHbTotal_RPOne dayAbsolute concentration of total hemoglobin: aHbTotal (μmol/L)
ΔO2Hb_RPOne dayOxygenated hemoglobin change: ΔO2Hb (μmol/L)
ΔHHb_RPOne dayDeoxygenated hemoglobin change: ΔHHb (μmol/L)
ΔcHb_RPOne dayTotal hemoglobin change: ΔcHb (μmol/L)
aHbDeoxy_RPOne dayAbsolute concentration of deoxygenated hemoglobin: aHbDeoxy (μmol/L)

Countries

Switzerland

Outcome results

None listed

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