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Stellate Ganglion Block and Prognosis of Neurological Function After Subarachnoid Hemorrhage

Effect of Stellate Ganglion Block on the Prognosis of Neurological Function After Subarachnoid Hemorrhage

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07652749
Enrollment
560
Registered
2026-06-17
Start date
2026-06-15
Completion date
2029-03-31
Last updated
2026-06-17

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

Conditions

Aneurysmal Subarachnoid Hemorrhage, Neurological Prognosis, Stellate Ganglion Block

Brief 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.

Interventions

PROCEDUREIntervention 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

Sponsors

Beijing Tiantan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 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.

Design outcomes

Primary

MeasureTime frameDescription
The modified Rankin Scale (mRS) scores at 90 days90 days postoperativelyThe 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.

Secondary

MeasureTime frameDescription
The incidence of delayed cerebral ischemia (DCI) during hospitalizationAt discharge, an average of 2 weeks
All cause mortality during 90 days after onset90 days postoperatively
Length of stay in the intensive care unit and hosipitalAt discharge, an average of two weeks
Adverse events during hospitalizationAt discharge, an average of 2 weeksMyocardial infarction, cardiac arrest, pulmonary embolism, infection, SGB related complications, etc

Countries

China

Contacts

CONTACTRuquan Han, M.D., Ph.D
ruquan.han@gmail.com8610-59976660
PRINCIPAL_INVESTIGATORRuquan Han, M.D., Ph.D

Beijing Tiantan Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 18, 2026