Hyperventilation Clinical Trial
— TCvsPETCO2Official title:
Transcutaneous Carbon Dioxide Pressure (tcPCO2) Monitoring Vs End-tidal Partial Pressure Carbon Dioxide (PetCO2) Measurement in the Diagnosis of Hyperventilation Syndrome (HVS) (TCvsPETCO2 )
Verified date | June 2020 |
Source | University Hospital, Rouen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Hyper Ventilation Syndrome is a frequent disease affecting adults whose diagnosis is often
belated or even unrecognized due to the lack of "gold standard" criteria. Its diagnosis
currently relies on the Nijmegen score associated with a PetCO2 assesment using a
hyperventilation provocation test. Correlation between Nijmegen Questionnaire scores and
PetCO2 appears highly variable. PtcCO2 monitoring is a noninvasive alternative method
providing a continuous estimation of arterial CO2 pressure (PaCO2) which could represent an
advantageous alternative to PetCO2 measurements. Several reports have demonstrated that
PtcCO2 monitoring reflects more faithfully PaCO2 than PetCO2, no study have evaluated its
value in this indication.
The primary aim of the study is to compare the diagnostic value of PtcPCO2 monitoring with
PetCO2, the method currently used.
Included patient will be invited to fill in the Nijmegen questionnaire and an ambient air gas
measurement will be performed. PtcCO2 (mmHg) will be simultaneously measured during
hyperventilation test. Nijmegen score signs reproduced by the test will be analysed. HVS
diagnosis will be assessed by usual criteria (PetCO2 <30 mmHg at the end of hyperventilation
test or under the PetCO2 value at rest, Nijmegen score> 23).
PtcCO2 data will be blinded interpreted later. We will compare if PetCO2 and PtcCO2 leads to
the same diagnosis or not.
Status | Completed |
Enrollment | 14 |
Est. completion date | February 15, 2018 |
Est. primary completion date | February 15, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: 1. The patient must have reached the age of the civil majority (= 18 yo) 2. All patients refered to the Physiology department of Rouen University Hospital, France, for an hyperventilation test 3. The patient must be a member or beneficiary of a health insurance program 4. The patient must have given his / her free and informed consent and signed the consent Exclusion Criteria: 1. Sepsis 2. Hypercapnia (PaCO2 > 50mmHg) 3. Patient treated by long-term oxygen therapy 4. Subjects under judicial protection, or adults under any kind of guardianship or under judicial control 5. Pregnancy or breastfeeding women 6. Electrolytic unbalance 7. Hyperthyroidism 8. Neurological disease 9. Probability of drug-induced hyperventilation (progestagens , aspirin, beta agonists) |
Country | Name | City | State |
---|---|---|---|
France | Physiology department of Rouen University Hospital, | Rouen |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Rouen |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Trans-cutaneous Carbon Dioxide pressure | Trans-cutaneous Carbon Dioxide pressure measurements diagnostic of hyperventilation syndrome will be evaluated by comparing it with that of standard | during hyperventilation test | |
Primary | End-tidal Carbon Dioxide partial pressure | End-tidal Carbon Dioxide partial pressure measurement. Consistency of the diagnostic conclusions reached by either test will be analyzed. | during hyperventilation test |
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