Pain Clinical Trial
— MEOPanxOfficial title:
Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care
Verified date | April 2019 |
Source | University Hospital, Toulouse |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The emergency setting, frequently associated with pain and the feeling of loss of control,
can cause anxiety in patients.
Reaction anxiety may be an appropriate response to an emergency; Nevertheless, attention must
be paid to the evaluation and management of the latter especially as anxiety and pain are
closely linked.
Status | Active, not recruiting |
Enrollment | 30 |
Est. completion date | September 2019 |
Est. primary completion date | September 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patient over 18 - Patient supported by a SMUR team from Toulouse - Patient receiving MEOPA during pre-hospital care (in the usual indications for pain relief or pain-induced care) - Patient having given his non-opposition to participate in the study Exclusion Criteria: - Any patient with a contraindication to MEOPA: - Patient requiring pure oxygen ventilation - Intracranial hypertension - Any alteration of the state of consciousness preventing the patient's cooperation - Traumatic brain injury - Pneumothorax - Emphysema bubbles - Gas embolism - Diving accident - Abdominal gas distension - Patient who received an ophthalmic gas for ocular surgery less than three months old - Known and unsubstituted vitamin B12 deficiency - Patient under legal protection - Refusal of the patient to participate in the study - Barrier of the language or alteration of the communication - Patient in vital distress |
Country | Name | City | State |
---|---|---|---|
France | University Hospital Toulouse | Toulouse |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Toulouse |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The state of anxiety of the patient assessed by Face Anxiety Scale | The state of anxiety of the patient assessed by FAS (face anxiety scale) self-assessment when supported by a SMUR team with MEOPA administration. The FAS, called the Anxiety Faces Scale, is a validated anxiety assessment scale that was originally developed in the context of Critical Care, Critical Care (ICU) management. The Faces Anxiety Scale is a valid single-item, self-report measure of state anxiety in intensive care patients that is easy to administer and imposes minimal respondent burden. It has the potential to be a useful instrument for the assessment of state anxiety by clinicians and for research into the reduction of anxiety in this vulnerable population. |
2 hours | |
Secondary | The pain felt by the patient, evaluated by the numerical scale (EN), in connection with his anxiety | EN is a self-rated scale of pain: the patient rates his or her pain on a numeric scale from 0 (no pain) to 10 (maximum pain). The evaluation of the pain at the SAMU is carried out in routine at each support by the EN. For the purposes of this study, the investigators will find the value of the EN in the same temporality as the assessment of anxiety. | 2 hours |
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