NCT05891509Recruiting
DTI-guided Minimally Invasive Hematoma Evacuation for Intracerebral Hemorrhage
Efficacy and Safety of DTI-guided Minimally Invasive Hematoma Evacuation Versus Best Medical Therapy for Acute Spontaneous Intracerebral Hemorrhage: a Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 13 Sept 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Intracerebral hemorrhage (ICH) is a devastating disease with high early mortality, unfavorable neurological outcomes, and high cost of care. To date, the role of DTI-guided minimally invasive hematoma evacuation in ICH is still uncertain. The investigators will conduct a multicenter randomized controlled trial, as well as a concurrent prospective observational study including all ICH patients who decline participation in the trial and will therefore receive minimally invasive hematoma evacuation or best medical therapy and consent to be followed up. All participants will be followed up at the same time using the same outcomes measures. The primary outcome will be collected by a blinded assessor.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- First submitted
- 28 May 2023
- Start date
- 3 Aug 2023
- Primary completion date
- 31 May 2027
- Lead sponsor
- Zhongming Qiu
- Diseases
- Stroke
- NCT number
- NCT05891509
What you commit to
- Study type: Interventional
- Planned participants: 100
- From 3 Aug 2023 to the primary completion date, 31 May 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous history of bleeding, such as gastrointestinal bleeding, genitourinary bleeding, respiratory bleeding that has not been completely controlled;
- Long-term anticoagulation and antiplatelet therapy are expected to be required;
Other illness
- Bleeding in other parts (e.g., bleeding in subtentorial areas such as thalamus, brainstem or cerebellum);
- Bleeding caused by other causes (such as aneurysm, arteriovenous malformation, brain trauma, brain tumor, bleeding transformation of large cerebral infarction, bleeding caused by β amyloidosis, bleeding caused by coagulation dysfunction) or combined with aneurysm, arteriovenous malformation, brain trauma, brain tumor, large-scale cerebral infarction, β amyloidosis, severe coagulation dysfunction;
- Multiple intracranial hemorrhage;
- Patients with ventricular hemorrhage or ICH rupture into the ventricles should consider the need for ventricular drainage;
- Any history of brain parenchymal or other intracranial subarachnoid, subdural or epidural hemorrhage and surgical history in the past 30 days;
- Myocardial infarction within the past 30 days;
- Allergy to alpeplase, urokinase or surgery-related drugs and instruments;
- Known high risk of embolism, including patients with mechanical heart valves implanted in the body, history of left heart thrombosis, mitral stenosis with atrial fibrillation, acute pericarditis, or subacute bacterial endocarditis. Atrial fibrillation without mitral stenosis is appropriate;
- hypertension (systolic blood pressure is still greater than 180mmHg) that cannot be effectively controlled by aggressive antihypertensive therapy before randomization;
- Life expectancy \< 12 months in the advanced stage of any disease;
Lab values
- Hemoglobin \< 100g/L, hematocrit \<25%, platelet count \< 100\*109/L;
- Receiving anticoagulant drugs such as warfarin, dabigatran or rivaroxaban within 1 week prior to enrollment, with an INR \> 1.4;
Other
- Pregnant or lactating women;
- Participating in other interventional clinical studies.
Who the study is looking for
- Age 18-80 years old;
- Intracerebral hemorrhage in the basal ganglia was diagnosed by CT examination;
- The amount of bleeding is 20-40ml, and the midline structure is displaced horizontally by \< 3mm in the pineal gland;
- The degree of integrity and continuity of the corticospinal tract on the lesion side of magnetic resonance diffusion tensor imaging was graded as grade 2\~4;
- The time from onset to randomization is within 24 hours;
- GCS score ≥ 4 points at randomization;
- Muscle strength level 3 in the affected limb;
- Written informed consent are provided by the patients or their legal representatives.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Xingguo County People's Hospital Coordinator of this site? Confirm its status | Ganzhou | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.