Skip to content

The Atorvastatin and Dexamethasone Treatment for Patients with Chronic Subdural Hematoma

The Atorvastatin and Dexamethasone Treatment for Patients with Chronic Subdural Hematoma

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-14005573
Enrollment
Unknown
Registered
2014-08-17
Start date
2014-06-01
Completion date
Unknown
Last updated
2019-02-04

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

Conditions

Chronic subdural hematoma

Interventions

Group 1:oral administration of Atorvastatin
Group 2:oral administration of Atorvastatin and Dexamethasone

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. To be aged from 18 to 90 years old, both gender; 2. CT scan reveals supratentorial, unilateral or bilateral chronic subdural hematoma (MRI scan is warranted if diagnosis is difficult); 3. The midline shift to less than 1 cm, exclude the patients with the risk of cerebral hernia; 4. Markwalder's Grading Scale and Glasgow Coma Scale (MGS-GCS) lower than Grade 3; 5. Attending physician makes a judgment that cerebral hernia would not occur and surgical operation might not be performed in a short time. Conservative treatment is adopted; 6. Patients have never undergo surgery on the hematoma; 7. Patient fully understood the nature of the study, and voluntarily participates and signs informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergic to the statin and dexamethasone or its ingredients; 2. Hematoma caused by tumors, blood and other known comorbidities; 3. Abnormal liver function; Uncontrolled hepatitis and other liver diseases, as well as suffering from other disease may interfere the study; 4. Patients have been on oral Statin in the past four weeks; 5. Patients have been on oral Steroids for a long time; 6. Diabetes diagnosis and patients with poorly controlled blood glucose; 7. Participate in clinical trials in the past four weeks; 8. Failure of completing the trial by poor compliance; 9. Hypertension is extremely high risk; 10. Merge infection without under control; 11. For any reason, the researchers believe that the case is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
the quantity change on CT before and after treatment hematoma;

Secondary

MeasureTime frame
the symptoms improve before and after every stage treatment;Blood routine before and after every stage treatment;Liver function before and after every stage treatment;Blood coagulation function;GOSE prognostic score;Daily life ability score (ADL score);

Countries

China

Contacts

Public ContactWang Dong

Tianjin Medical University General Hospital

54454241@qq.com+86 13920732851

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026