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Starting soon Not applicable

Stellate Ganglion Block and Prognosis of Neurological Function After Subarachnoid Hemorrhage

NCT07652749 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2026-06-15
Last updated
2026-06-17

Condition(s) studied

Aneurysmal Subarachnoid HemorrhageStellate Ganglion BlockNeurological Prognosis

Investigational drug(s) / intervention(s)

Intervention group

Intervention group: Prior to the initiation of surgery, a single ultrasound-guided stellate ganglion block was performed on the ipsilateral side of the lesion.The dose and concentration of local anesthesia: 0.5% ropivacaine 5-10ml. Criteria for successful block: the patient developed Horner's syndrome, characterized by miosis, ptosis, eyeball caved in, nasal congestion, conjunctival congestion, reddish face and no sweat on the face

Study summary

The incidence of cerebral vasospasm after aneurysm subarachnoid hemorrhage (aSAH) is as high as 70%; cerebral vasospasm(CVS) is closely related to delayed cerebral ischemia (DCI), which is one of the important reasons for poor outcomes in patients with aSAH.

In recent years, it has been reported that stellate ganglion block(SGB) can effectively alleviate cerebral vasospasm(CVS), reduce cerebral blood flow velocity and increase cerebral perfusion in patients with aneurysm subarachnoid hemorrhage(aSAH)。However, whether the alleviation of CVS after SGB is beneficial to the long-term neurological prognosis has not been confirmed Therefore, a prospective randomized controlled study is needed to further explore the role of SGB block in improving the outcomes of patients with aSAH.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age range: 18-65 years old; * Within 72 hours after onset of aSAH,and planning surgical treatment(aneurysm embolizing or clipping); * Preoperative Hunt-Hess grade 2-3 * Sign informed consent. Exclusion Criteria: * ASA \> grade IV; * Patients with posterior circulation aneurysm; * Patients with severe systemic hemorrhagic diseases; * Patients with trauma and local infection in the nerve block area; * Local anatomic structure changes (neck structure changes caused by radiotherapy, chemotherapy and surgery); * Allergy to known local anesthetics; * Pregnant and lactating women.

Primary outcome measure(s)

  • The modified Rankin Scale (mRS) scores at 90 days — 90 days postoperatively
    The modified Rankin Scale (mRS) is used to evaluate the primary outcome. The scale of mRS is 0 to 6. The best neurological outcome is the mRS with 0, indicating no any symptom left. mRS of 6 is the worst, indicating death. mRS will be evaluated by outcomes assessor who is blinded to the grouping.

Trial sites (1)

FacilityCityRegionStatus
Beijing Tiantan Hospital, Capital Medical University Beijing Beijing Municipality
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07652749 on ClinicalTrials.gov ↗ ← All trials in China