Actively Recruiting
Neuroendoscopy-assisted Drainage Versus Burr Hole Drainage for Chronic Subdural Hematoma
Led by Beijing Tiantan Hospital · Updated on 2026-02-09
770
Participants Needed
24
Research Sites
110 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Chronic subdural hematoma (CSDH) is a frequent condition in neurosurgery, leading to fluid accumulation between the meninges, brain compression, neurological dysfunction, and potentially herniation. The efficacy of treatments and their long-term outcomes remain uncertain, with no established standard. Notably, neuroendoscopy-assisted hematoma evacuation, in contrast to burr-hole drainage, enables direct visualization and thorough removal of the hematoma, thereby minimizing residue, lowering recurrence rates, and shortening drainage duration. This study will undertake a multicenter trial to compare these two methods and determine the superior treatment approach for CSDH.
CONDITIONS
Official Title
Neuroendoscopy-assisted Drainage Versus Burr Hole Drainage for Chronic Subdural Hematoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 90 years with symptoms and neurological deficits of chronic subdural hematoma
- Diagnosis of chronic subdural hematoma confirmed by cranial CT or MRI
- Written informed consent from the patient or their legal representative if the patient is cognitively impaired
You will not qualify if you...
- No clinical symptoms related to chronic subdural hematoma
- No mass effect or midline shift less than 5 mm on imaging, or surgery not clinically needed
- Previous surgery for chronic subdural hematoma within the last 6 months
- Previous intracranial surgery for other neurological disorders
- Severe health conditions or comorbidities preventing surgery or follow-up
- Severe bleeding disorders or high risk of life-threatening bleeding as defined by specific blood test criteria
- Unlikely to comply with 3-month follow-up visits
- Women of reproductive age without negative pregnancy test
- Participation in another research study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 24 locations
1
Beijing Tiantan Hospital, Capital Medical University
Beijing, Beijing Municipality, China, 100070
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2
First Affiliated Hospital of Xiamen University
Xiamen, Fujian, China, 361003
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3
Jiangmen Central Hospital
Jiangmen, Guangdong, China, 529030
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4
Shantou central hosital
Shantou, Guangdong, China, 515031
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5
People's Hospital of Longhua, Shenzhen
Shenzhen, Guangdong, China, 518109
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6
Liuzhou worker's Hospital
Liuzhou, Guangxi, China, 545007
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7
The Second Affiliated Hospital of Guangxi Medical University
Nanning, Guangxi, China, 530006
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8
Nanning First People's Hospital
Nanning, Guangxi, China, 530016
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9
The First Affiliated Hospital of Guangxi University of Traditional Chinese Medicine
Nanning, Guangxi, China, 530023
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10
Wuzhou Gongren Hospital
Wuzhou, Guangxi, China, 543001
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11
Hebei University of Engineering Affiliated Hospital
Handan, Hebei, China, 056002
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12
Xingtai Central Hospital
Xingtai, Hebei, China, 054099
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13
Changde First People's Hospital
Changde, Hunan, China, 415003
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14
People's Hospital of Xiangxi Prefecture, Hunan Province
Jishou, Hunan, China, 416007
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15
Yueyang Central Hospital
Yueyang, Hunan, China, 414020
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16
Heji Hospital affiliated with Changzhi Medical College
Changzhi, Shanxi, China, 046011
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17
Linfen People's Hospital
Linfen, Shanxi, China, 041000
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18
Shanxi Provincial People's Hospital,Shanxi Medical University
Taiyuan, Shanxi, China, 030012
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19
The Second Affiliated Hospital of Xi'an Medical University
Xi’an, Shanxi, China, 710038
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20
Mianyang 404 Hospital
Mianyang, Sichuan, China, 621000
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21
the First People'S Hospital of Yibin
Yibin, Sichuan, China, 644606
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22
First Affiliated Hospital of Xinjiang Medical University
Ürümqi, Xinjiang, China, 830054
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23
Pu'er People's Hospital
Pu'er, Yunnan, China, 665099
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24
First Affiliated Hospital of Wenzhou Medical University
Wenzhou, Zhejiang, China, 325000
Actively Recruiting
Research Team
L
Liang Wu, MD
CONTACT
Y
Yu Yan, MB
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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