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Clot-Busting drugs may cut death risk in lung clot patients

NCT ID NCT07374978

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether giving clot-busting drugs (thrombolysis) to people with a serious but not immediately life-threatening type of lung clot (pulmonary embolism) and a low risk of bleeding could lower their chance of dying within 30 days. The study included 100 patients and tracked deaths and major bleeding events. The goal was to see if the benefits of breaking up the clot outweigh the risks of bleeding.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

100 people

The number who actually took part.

Started

Jul 2023

Finished

Jul 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

25 to 70 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients with intermediate high risk pulmonary embolism diagnosed according to clinical probability using revised Geneva Score and diagnosis confirmed by echocardiography and Troponin I or T level and CT pulmonary angiography Exclusion Criteria: * o High risk PE * Intermediate low risk PE * low risk PE * Patients with left ventricular systolic dysfunction (ischemic or non-ischemic etiology) * Patients with chronic lung diseases (obstructive or restrictive) * Patients with contraindications to thrombolysis: * History of haemorrhagic stroke or stroke of unknown origin * Ischaemic stroke in previous 6 months * Central nervous system neoplasm * Major trauma, surgery, or head injury in previous 3 weeks * Bleeding diathesis (known inherited bleeding disorder, for example, haemophilia, platelet count \<50,000/uL) * Active bleeding * Transient ischaemic attack in previous 6 months * Oral anticoagulation * Pregnancy or first post-partum week * Non-compressible puncture sites * Traumatic resuscitation * Severe hypertension (systolic BP \>180 mmHg) * Advanced liver disease * Infective endocarditis * Active Peptic ulcer * Patients who develop hypotension or bradycardia or allergic reaction requiring discontinuation of Streptokinase infusion. * Patients with HAS-BLED score greater than or equals 3 (high bleeding risk for thrombolysis)

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Ain Shams University

    Cairo, Abbassia, 00202, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.