Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
NCT06401772

The Effectiveness and Safety of Body Posture in Preventing Postoperative Recurrence for Chronic Subdural Hematoma

Led by Huashan Hospital · Updated on 2026-04-30

830

Participants Needed

1

Research Sites

177 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the effectiveness and safety of body posture to improve intracranial pressure in preventing postoperative recurrence for chronic subdural hematoma

CONDITIONS

Official Title

The Effectiveness and Safety of Body Posture in Preventing Postoperative Recurrence for Chronic Subdural Hematoma

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with chronic subdural hematoma by CT or MRI with hematoma thickness over 1 cm
  • Age 60 years or older
  • Markwalder's Grading Scale and Glasgow Coma Scale score less than or equal to 2
  • Presence of neurological symptoms caused by chronic subdural hematoma before surgery, such as headache, dizziness, nausea, vomiting, numbness or weakness of limbs, instability while walking, unconsciousness, trouble speaking, or insensitivity
  • Received burr hole drainage surgery
  • Signed informed consent voluntarily
Not Eligible

You will not qualify if you...

  • Brain hernia or acute massive cerebral infarction requiring craniotomy
  • Severe malignancies, hemorrhagic disease, cardiac dysfunction, or other serious diseases that may hinder recovery or follow-up
  • Spinal deformities or psychiatric disorders preventing adherence to body posture therapy
  • Severe intracranial tumors, aneurysms, or vascular malformations affecting recovery
  • Cranial CT showing no significant brain compression or displacement, asymptomatic, and unaffected daily activities, making surgical intervention unsuitable
  • Chronic subdural hematoma persisting over 1 year with marked hematoma solidification
  • Chronic subdural hematoma caused by over ventriculoperitoneal shunting
  • Need for craniotomy during burr hole drainage due to acute bleeding or brain hernia
  • Intraoperative complications such as cerebral contusion or intraparenchymal catheter placement during burr hole drainage
  • Deep venous thrombosis of lower extremity or pulmonary embolism
  • Inability to complete regular reexaminations within 1 year
  • Life expectancy less than 1 year
  • Participation in other ongoing clinical trials
  • Not qualified for other reasons as evaluated by two neurosurgeons
  • Presence of bile reflux gastritis or esophageal diseases

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Department of Neurosurgery, Huashan Hospital, Fudan University

Shanghai, Shanghai Municipality, China, 200000

Actively Recruiting

Loading map...

Research Team

X

Xuehai Wu, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here