Different Treatment Strategies on Prognosis of Acute Ischemic Stroke(AISDTS)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNanjing First Hospital, Nanjing Medical University

About this trial

AISDTS is a prospective registry study, in which clinical information, examination and imaging data of patients with acute ischemic stroke receiving different treatment strategies were collected, grouped and statistically analyzed, and corresponding clinical prediction models were constructed to explore the role of clinical biological indicators in the occurrence and development of stroke.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

A) ≥18 years of age; B) hospital admission for ischemic stroke; C) Signed informed consent.

Disqualifiers

A) patients with incomplete clinical information; B) hospitalization observation time less than 24 hours; C) recent trauma, severe inflammation, severe liver and kidney dysfunction, progressive malignance and other serious diseases; D) baseline mRS score>2; E) informed consent is not signed.

Trial population

Patients admitted to hospital for ischemic stroke were enrolled.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

5,000 Participants
are grouped into 6 trial groups

6

Trial groups

See each trial group below.

Group A: thrombolysis group
Group B: thrombectomy group
Group C: stent group
Group D: regular treatment group
Group E: young stroke group
Group F: unexplained stroke group

Trial outcomes

Primary outcomes

1

To assess the changes of prognosis of stroke patients under different treatment strategies

assessed by The Modified Rankin Score (mRS) of stroke patients \[mild to wores ranging from 0 to 5, 6 represents death\].

Time frame
3 months, 6 months, 12 months or 24 months
2

To assess the early neurological changes of ischemic stroke

change from baseline National Institute of Health stroke scalescore (NIHSS) \[higher scores mean worse conditions\]7 days or 14 days

Time frame
7 days or 14 days

Secondary outcomes

1

To assess the incidence of recurrent stroke under different treatment strategies

record and analyze the incidence of recurrent stroke from 7 days-24 months

Time frame
7 days-24 months
2

To assess the types and incidence of adverse events of ischemic stroke patients

adverse reactions (hemorrhage, embolus shedding, gastrointestinal ulcer) and stroke-related complications under different treatment strategies

Time frame
3 days-24 months
3

To assess the correlation of RNA/DNA and age factor in acute ischemic stroke

DNA and RNA extracted from peripheral blood samples

Time frame
3 months
4

To assess the therapeutical effects of Edaravone dexborneol on inflammation and prognosis after acute ischemic stroke

The Modified Rankin Score score (mRS) of stroke patients \[mild to wores ranging from 0 to 5, 6 represents death\].

Time frame
3 months

Other outcomes

Sponsors and contacts

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