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Multicenter prospective cohort study for the prevention and treatment of hydrocephalus after acute cerebral hemorrhage with traditional Chinese medicine

Multicenter prospective cohort study for the prevention and treatment of hydrocephalus after acute cerebral hemorrhage with traditional Chinese medicine

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR1900002389
Enrollment
Unknown
Registered
2019-06-09
Start date
2019-06-30
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

hydrocephalus after acute cerebral hemorrhage

Interventions

Sponsors

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine (Sichuan Traditional Chinese Medicine Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) The first time onset cerebral hemorrhage; (2) Meet the diagnostic criteria for cerebral hemorrhage, and the GCS score is >4 points; (3) Aged 40 and 75 years old; (4) Agree to participate in the trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) The patient's cerebral hemorrhage is caused by brain tumor, brain trauma, blood disease (secondary to anticoagulant and thrombolytic therapy); (2) with a mixed stroke or cerebral hemorrhage with severe bleeding needs to surgery; (3) The clinical manifestations of cerebral palsy, including the disappearance of ipsilateral pupillary reflexes and other third pairs of cranial nerve paralysis; (4) with pulmonary heart disease, unstable angina or acute myocardial infarction within 6 months; (5) with neurological deficits (mRS>2) before the onset of AICH; (6) Accompanied by severe cardiac insufficiency (NYHA cardiac function classification III-IV); (7) Accompanied by severe hepatic insufficiency (the liver function test results exceed 2 times the upper limit of the normal range); (8) Accompanied by severe renal insufficiency (the serum creatinine is more than twice the upper limit of the normal range); (9) Active gastrointestinal bleeding occurs after the onset of AICH in patients; (10) The patient has a heavier blood system or other systemic underlying disease; (11) The patient is in a state of pregnancy or breastfeeding, or has a severe allergic disease or is allergic to multiple drugs; (12) The patient has other diseases that cause his neurological deficit, or join the study to aggravate his condition; (13) The patient has participated in other clinical trials in the past 3 months; (14) Patients without malignant tumors and receiving radiotherapy and chemotherapy

Design outcomes

Primary

MeasureTime frame
Hematoma volume;NIHSS score;The incidence of hydrocephalus after acute cerebral hemorrhage in two cohorts;Hematoma volume;

Secondary

MeasureTime frame
The occurrence of death endpoints in each study cohort from the implementation of the program to the end of treatment;Quality of life indicator;

Countries

China

Contacts

Public ContactLu Yun

Hospital of Chengdu University of Traditional Chinese Medicine

luyun999@126.com+86 18980880121

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026