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NCT06668441

Minimally Invasive Surgery and rhTNK-tPA for Intracerebral Hemorrhage Evacuation

Completed Phase 1 Last updated 7 March 2025
What this trial tests

Phase 1 trial testing Minimally invasive surgery plus low-dose rhTNK-tPA group in Intracranial Hemorrhages in 12 participants. Completed in 27 January 2025.

Timeline
4 November 2024
Primary endpoint
27 January 2025
27 January 2025

Quick facts

Lead sponsorBeijing Tiantan Hospital
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsequential
Maskingnone
Primary purposetreatment
Enrollment12
Start date4 November 2024
Primary completion27 January 2025
Estimated completion27 January 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Beijing Tiantan Hospital

Who can join

Adults 18 to 80, any sex, with Intracranial Hemorrhages or Cerebrovascular Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this trial is to determine the safety of using a combination of robot-assisted stereotactic puncture and clot lysis with rhTNK-tPA to remove intracerebral hemorrhage (ICH) and to provide dose evidence for a phase III clinical trial.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Phase I dose-escalation study of tenecteplase, a third-generation fibrinolytic agent, combined with neuronavigation-assisted stereotactic minimally invasive puncture, in patients with acute spontaneous deep cerebral haemorrhage.
    Wu Z, Wang M, Bai X, Tang J, et al · · 2025 · PMID 40992931 · DOI 10.1136/svn-2025-004389

Verify or expand the search:

Other recruiting trials for Intracranial Hemorrhages

Currently open trials in the same condition.

Other Beijing Tiantan Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06668441.

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