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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04512859
Other study ID # 20200630
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date December 31, 2022

Study information

Verified date September 2020
Source Beijing Tiantan Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To investigate whether the stellate ganglion block is helpful in relieving cerebral vasospasm during aneurysmal coil embolism surgery. The effect was assessed by Transcranial Doppler (TCD).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 160
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- 1.Emergency patients with subarachnoid hemorrhage caused by ruptured aneurysm, aged 18-65 years; 2. ASA : II-IV grade, Hunt-Hess : I-III grade 3. For the first case, the operation time is within 24 hours. 4.After signing informed consent, underwent interventional intravascular embolization

Exclusion Criteria:

- 1. Patients with severe bleeding disorders; 2. Patients with trauma and local infection risk in the nerve block area; 3. Patients with previous aneurysm surgery and unruptured aneurysm; 4. Aneurysm located in middle cerebral artery; 5. Patients with unconsciousness cannot cooperate with the block operation; 6. Those with a history of mental illness and epilepsy; 7. Those who have a history of severe cardiovascular and cerebrovascular diseases and severe organ diseases;

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Stellate Ganglion Block
Stellate ganglion block under ultra-guide will be administered using 0.25% ropivacaine 10mL
Placebo
Stellate ganglion block under ultra-guide will be administered using 0.9% saline 10mL

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Beijing Tiantan Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary The incidence of cerebral vasospasm Change from baseline at 5day,after subarachnoid hemorrhage
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