Skip to content

Intravenous Tenecteplase (TNK) in Acute Ischemic Stroke: a multicenter, prospective registry

Intravenous Tenecteplase (TNK) in Acute Ischemic Stroke: a multicenter, prospective registry

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102308
Enrollment
Unknown
Registered
2025-05-13
Start date
2024-09-11
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Acute ischaemic stroke

Interventions

Observation group:None

Sponsors

Beijing Daxing District People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1) Age >= 18 years old; 2) Acute ischemic stroke was diagnosed; 3) Thrombolytic therapy with Teneplase (rhTNK-tPA); 4) Patients or their representatives sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Use of other thrombolytic drugs (alteplase, urokinase, etc.); 2) Pregnant or breastfeeding women; 3) Unable to comply with the study protocol or follow-up requirements; 4) The investigator deems it inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
90-day modified Rankin (mRS) score on a scale of 0-1 points;DNT:door to needle time;

Secondary

MeasureTime frame
90-day modified Rankin (mRS) score on a scale of 0-2 points;90-day modified Rankin (mRS) score displacement analysis;Improvement in NIHSS score at 7 days/discharge from baseline (NIHSS score 0-1 or NIHSS score is base line improvement =4 points).;Symptomatic intracranial hemorrhage within 24 hours;Incidence of intracranial hemorrhage within 90 days;Incidence of bleeding at any site within 90 days;90-day mortality;DPT:Door-to-Puncture Time;Time to thrombolysis to femoral artery puncture (for patients treated with bridging);

Countries

China

Contacts

Public ContactJinglin Yuan

Beijing Daxing District People’s Hospital

Yuanjl@126.com+86 134 2625 2069

Outcome results

None listed

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