Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:03 PM
Ignite Modification Date:
2025-12-24 @ 1:03 PM
NCT ID:
NCT06735261
Eligibility Criteria:
Inclusion Criteria:
* ≥ 18 years
* Non-traumatic SAH with or without aneurysm on brain imaging
* WFNS score 1 and 2
* Patient awake and extubated after radiological procedure
* Patient in pain (EN \> 3/10) despite usual level 1 analgesics (Paracetamol + Acupan)
* Affiliated with or benefiting from a social security scheme
Exclusion Criteria:
* Contraindication to sphenopalatine ganglion block (deviated nasal septum, repeated epistaxis, allergy to Lidocaine)
* Patient unable to assess pain by EN
* Persons covered by Articles L1121-5 to L1121-8 of the CSP and Articles 31 to 35 of Regulation 536/2014.
* Participation in other interventional research
* Patient's refusal to participate
* Arteriography more than 48 hours old
* Inaugural headache lasting more than 48 hours
* Presence of an unsecured vascular malformation at high risk of rupture
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06735261
Study Brief:
Protocol Section:
NCT06735261