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An observational study on the effect of edaravone and dexcamphenol combined with recanalization on the expression of serum inflammatory factors and prognosis in patients with acute ischemic stroke

An observational study on the effect of edaravone and dexcamphenol combined with recanalization on the expression of serum inflammatory factors and prognosis in patients with acute ischemic stroke

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055910
Enrollment
Unknown
Registered
2022-01-23
Start date
2022-01-25
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Acute ischemic stroke

Interventions

treatment group:Edaravone and Dexborneol Concentrated Solution for Injection +Recanalization therapy(Intravenous thrombolysis / intravascular therapy)
Control group:conventional therapy +Recanalization therapy(Intravenous thrombolysis / intravascular therapy)

Sponsors

Putian First Hospital, Fujian Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 80 years; 2.Stroke diagnosis determined by the Fourth Academic Conference on cerebrovascular diseases in 1995 Standard, combined with clinical symptoms and imaging examination; 3.Onset time < 48 hours; 4.Meet the indications of intravenous thrombolysis and receive intravenous thrombolysis; Or cranial CTA or MRA or DSA showed obstruction of large blood vessels (ICA, mca-m1, ACA, PCA, BA) and received intravascular intervention; 5.6 <= NIHSS score <= 25; 6.mRS score before onset <= 1; 7.The patient/family member signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Previous mental illness or cognitive impairment, unable to live normally or cooperate with the researcher; 2.Contraindication of Edaravone and right camphor; 3.Those who refuse or cannot effectively cooperate with the treatment; 4.Other unwilling to participate in the research.

Design outcomes

Primary

MeasureTime frame
The rate of good prognosis after 90 days.(mRs=2);

Secondary

MeasureTime frame
Changes of plasma inflammation markers;

Countries

China

Contacts

Public ContactChen Ping

Putian First Hospital, Fujian Province

edmunc@sina.com+86 15960523537

Outcome results

None listed

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