Phase 3 Stroke Trial, Recruiting NCT07141303 Sponsor: Tang-Du Hospital Condition: Stroke
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Phase 3 Stroke Trial, Recruiting

NCT07141303
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged between 18 and 80 years old
  • People whose stroke symptoms started no more than 24 hours before being enrolled in the trial
  • People who have had a stroke caused by a blockage in a major blood vessel at the front of the brain, confirmed by a specialised brain scan (such as CTA, MRA, or DSA)
  • People whose stroke symptoms are linked to that specific blocked blood vessel
  • People with a stroke severity score (called NIHSS) of 6 points or higher, indicating a moderate to severe stroke
  • People whose brain scan (NCCT) shows an ASPECTS score of 3 or higher, which is a measure of how much brain tissue has been affected
  • People who have already had a successful procedure to remove the blood clot from the blocked vessel (called endovascular thrombectomy), with a good result on a standard medical scale
  • People, or their family members, who have signed a written consent form agreeing to take part

Who may not be able to join:

  • People who have bleeding in the brain, confirmed by a CT or MRI scan
  • People who already had some level of disability before the stroke (a pre-stroke disability score of 2 or higher on a standard scale)
  • People who are pregnant or breastfeeding
  • People with a known allergy to iodine-based contrast dye, or to the medication methylprednisolone sodium succinate
  • People who are already taking part in another clinical trial
  • People with a blood clotting disorder (either inherited or acquired), or who are taking blood-thinning medication with a clotting measure (INR) above 1.7
  • People who have had a major bleeding episode in the past month, such as bleeding in the stomach, bowel, or urinary tract
  • People on regular kidney dialysis, or with severely reduced kidney function (based on specific blood or filtration measurements)
  • People with a terminal illness where life expectancy is less than 6 months
  • People with blood sugar levels that are either too low (below 2.8 mmol/L) or too high (above 22.2 mmol/L)
  • People found to have a brain aneurysm, an abnormal tangle of blood vessels (arteriovenous malformation), or a brain tumour that is pressing on surrounding brain tissue
  • People with an active infection anywhere in the body
  • People who are unlikely to be able to complete the required follow-up appointments
  • People in whom a scan during the clot-removal procedure showed a blood vessel tear, puncture, or leakage of dye
  • People whose clot-removal procedure took longer than 90 minutes from first access to reopening the vessel, or required more than 3 attempts to remove the clot

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 6 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 0086-18729985168

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Tang-Du Hospital
Registry
ClinicalTrials.gov
Start date
8 August 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Shift in the distribution of mRS scores; Incidence of symptomatic intracranial hemorrhage; Mortality

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 6 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov