Clinical Trials Directory

Trials / Completed

CompletedNCT00966316

Establishment and Evaluation to the Effects of a Clinical Pathway for Acute Ischemic Stroke

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
314 (actual)
Sponsor
Guangzhou University of Traditional Chinese Medicine · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether the clinical pathway for acute ischemic stroke(with combination of traditional Chinese medicine and western medicine) is able to improve the outcome of acute ischemic stroke and evaluate its effect on hospital day and cost, etc. Meanwhile, the study will discuss the safety and efficiency of this kind of Clinical Pathway

Detailed description

Eligibility Ages Eligible for Study: 18 Years to 85 Years Genders Eligible for Study: Both Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Those clinically diagnosed with acute ischemic stroke ; 18-85 years old; Over 6 hours and within 14 days from onset 4\<=NIHSS \<=22; Informed consent signed by patient or his/her family ; Exclusion Criteria: Hemorrhagic stroke; Cerebral hernia; Serious heart, liver, lung, kidney functional failure,malignancy; Not cooperative with physician; Psychological disorder; Already taken part in other clinical drug trial within the past 3 months

Conditions

Interventions

TypeNameDescription
DRUGaspirin,chinese herbs;aspirin 300mg/100mg,qd,chinese herbs, one dose ,qd

Timeline

Start date
2009-05-01
Primary completion
2010-08-01
Completion
2011-01-01
First posted
2009-08-26
Last updated
2011-05-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00966316. Inclusion in this directory is not an endorsement.