- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07651631
Rapid Evacuation and Access of Cerebral Hemorrhage Registry (REACH)
A Prospective, Multicenter, Global Registry Evaluating Minimally Invasive Surgery for the Treatment of Acute Spontaneous Supratentorial Intracerebral Hemorrhage.
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
Intracerebral hemorrhage (ICH) is one of the most severe forms of stroke, accounting for nearly one-third of all strokes worldwide and affecting more than 3 million people annually. It remains associated with high mortality-over 40% of patients die within 30 days-and significant long-term disability among survivors. Basal ganglia hemorrhage is the most common location of spontaneous ICH and often results in profound neurological deficits, including weakness, sensory loss, visual impairment, and cognitive or speech difficulties. In the United States, more than 80,000 patients each year experience an acute ICH, and the condition contributes substantially to years of life lost, particularly among adults aged 35-65.
Despite decades of research, treatment options for ICH remain limited. Standard medical management focuses on blood pressure control, reversal of coagulopathy, prevention of hematoma expansion, and management of intracranial pressure. Traditional open craniotomy has not consistently improved functional outcomes and carries risks such as infection, rebleeding, and prolonged recovery. As a result, interest has grown in minimally invasive surgical (MIS) techniques designed to remove the hematoma while minimizing damage to surrounding brain tissue.
Over the past two decades, several MIS approaches have been developed, including catheter-based aspiration with thrombolytics, neuroendoscopic evacuation, minimally invasive puncture and drainage, and navigated trans-sulcal parafascicular surgery using tubular retractors. These techniques aim to reduce surgical trauma, improve hematoma evacuation, and limit secondary brain injury caused by inflammation, oxidative stress, and perihematomal edema.
Recent randomized trials have provided important insights into the potential benefits of MIS. The MISTIE III trial demonstrated procedural safety and suggested improved outcomes in patients who achieved substantial hematoma reduction. The ENRICH trial showed that early minimally invasive parafascicular surgery improved functional outcomes at 180 days for patients with lobar ICH and reduced mortality, ICU stay, and serious adverse events. Other trials, including MIND and SWITCH, have contributed additional data on safety, short-term disability, and the potential role of MIS in deep hemorrhages. Updated guidelines from the European Stroke Organization and the American Heart Association now support consideration of MIS for selected patients with supratentorial ICH.
Although evidence is growing, real-world practice varies widely due to differences in patient selection, surgical expertise, device availability, and institutional protocols. Randomized trials often include highly selected populations, limiting generalizability. There is a need for large-scale, prospective, real-world data to better understand how MIS is used across diverse clinical settings and to identify which patients benefit most.
The Rapid Evacuation and Access of Cerebral Hemorrhage (REACH) Registry is designed to address these gaps by prospectively collecting standardized data on patients undergoing MIS evacuation for spontaneous supratentorial ICH. The registry will capture patient demographics, comorbidities, hematoma characteristics, surgical techniques, timing of intervention, degree of hematoma evacuation, and clinical outcomes including mortality, complications, and functional status. By aggregating real-world data across multiple centers, the registry aims to evaluate the safety and effectiveness of different MIS approaches, identify predictors of favorable recovery, and support ongoing improvements in clinical practice.
Ultimately, the REACH Registry seeks to advance evidence-based care for patients with ICH, inform future clinical trials, and contribute to the refinement of national and international treatment guidelines
Studientyp
Einschreibung (Geschätzt)
Kontakte und Standorte
Studienkontakt
- Name: Alex Hall, DHSc
- Telefonnummer: 404-778-1585
- E-Mail: alex.hall@emory.edu
Studienorte
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Georgia
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Atlanta, Georgia, Vereinigte Staaten, 30303
- Rekrutierung
- Grady Memorial Hospital
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Hauptermittler:
- Jonathan Ratcliff, MD, MPH
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Kontakt:
- Alex Hall, DHSc, MS
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Hauptermittler:
- Alex Hall, DHSc, MS
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- Head CT demonstrating an acute, spontaneous, intracerebral hemorrhage
- Hemorrhage volume ≥ 20 mLs
- Minimally invasive surgical intervention performed within 7 days of hemorrhage
Exclusion Criteria:
- Ruptured aneurysm, arteriovenous malformation (AVM), vascular anomaly, moyamoya disease, venous sinus thrombosis, mass or tumor, hemorrhagic conversion of an ischemic infarct, recurrence of a recent ICH (<1 year), as diagnosed with radiographic imaging
- Infratentorial intraparenchymal hemorrhage, including midbrain, pontine, or cerebellum
- Initial hospital arrival ≥ 24 hours after the onset of stroke symptoms
- Last known normal is unknown
- Historical Modified Rankin Score > 4
- Known life-expectancy of less than 1 year prior to ICH
- DNR or comfort measures only
- Known pregnancy in female subjects
- Inability or unwillingness of subject or legal guardian/representative to give written informed consent within 7 days of initial hospital arrival
- Inability to meet follow up requiremen
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Kohorten und Interventionen
Gruppe / Kohorte |
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Minimally Invasive Surgical Groups
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Control Group
No minimally invasive surgical hematoma evacuation performed; n=300 total, capped across 20 sites; may include patients undergoing decompressive hemicraniectomy or other standard medical/surgical approaches):
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Modified Rankin Scale (mRS) at 180 Days
Zeitfenster: Day 180 from baseline (±14 days)
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Functional outcome will be assessed using the modified Rankin Scale (mRS), a 7-level ordinal scale ranging from 0 (no symptoms) to 6 (death). The primary endpoint evaluates real-world functional recovery following minimally invasive surgery (MIS) for acute supratentorial ICH. Structured interview performed in person or via telephone by trained study personnel; audio-recorded and centrally adjudicated. |
Day 180 from baseline (±14 days)
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30-Day Mortality
Zeitfenster: Day 30 (±7 days)
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All-cause mortality within 30 days of the initial hemorrhage.
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Day 30 (±7 days)
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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modified Rankin Scale (mRS) at Additional Time Points
Zeitfenster: Day 7, 30, 90, 180, 365
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The endpoint evaluates real-world functional recovery following minimally invasive surgery (MIS) for acute supratentorial ICH.
Collected over phone or in-person via structured interview.
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Day 7, 30, 90, 180, 365
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Post-Operative Infection or CSF Leak
Zeitfenster: Baseline through Day 365
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Incidence of surgical site infection or cerebrospinal fluid leak.
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Baseline through Day 365
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Quality of Life (EQ-5D-5L)
Zeitfenster: Day 7, 30, 90, 180, 365
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The EQ-5D-5L assesses health status across five dimensions:
Each dimension has five levels (no problems, slight problems, moderate problems, severe problems, extreme problems), allowing patients to describe their health using a five-digit health state (e.g., 11223). Patients also complete a Visual Analogue Scale (VAS) rating their overall health from 0 (worst imaginable) to 100 (best imaginable) |
Day 7, 30, 90, 180, 365
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Follow-Up Neuroimaging (24-Hour)
Zeitfenster: Within 24 hours post-procedure
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Assessment of hematoma evacuation effectiveness and residual volume.
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Within 24 hours post-procedure
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In-Hospital Mortality
Zeitfenster: From date of enrollment through the date of hospital discharge (upto 14 days)
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All-cause mortality occurring during the initial hospitalization.
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From date of enrollment through the date of hospital discharge (upto 14 days)
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Change in Hematoma Volume
Zeitfenster: Baseline to follow-up imaging (within first 10 days)
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Difference between initial hematoma volume and follow-up neuroimaging volume, assessed centrally by the Neuroimaging Core Lab.
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Baseline to follow-up imaging (within first 10 days)
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Post-Operative Rebleeding With Neurologic Deterioration (Surgery Group Only)
Zeitfenster: Baseline through Day 10
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Rebleeding is defined as hematoma growth on follow-up imaging accompanied by neurologic decline (National Institute of Health Stroke Scale (NIHSS) increase ≥4 or Glasgow Coma Score (GCS) decrease ≤2)
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Baseline through Day 10
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Time to Intervention
Zeitfenster: From time of enrollment through the time of procedure (upto 100 days)
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Time from ictus (symptom onset) to MIS procedure.
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From time of enrollment through the time of procedure (upto 100 days)
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Surgical Complications
Zeitfenster: Baseline through Day 365
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Any intraoperative or postoperative complication related to Minimally invasive surgery (MIS) technique, including device-related events.
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Baseline through Day 365
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Residual Post-Operative Hemorrhage Volume
Zeitfenster: Post-operative imaging (≤10 days)
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Quantification of remaining hematoma volume after MIS.
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Post-operative imaging (≤10 days)
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Serious Adverse Events (SAEs)
Zeitfenster: Baseline through Day 365
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SAEs include events resulting in death, life-threatening conditions, hospitalization, disability, or events requiring medical/surgical intervention.
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Baseline through Day 365
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Hospital Length of Stay
Zeitfenster: From date of enrollment to the date of discharge (upto 4 weeks or more)
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Total number of days from hospital admission to discharge.
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From date of enrollment to the date of discharge (upto 4 weeks or more)
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Decompressive Hemicraniectomy
Zeitfenster: Baseline through discharge (upto 100 days or more)
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Receipt of decompressive hemicraniectomy during the initial hospitalization.
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Baseline through discharge (upto 100 days or more)
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ICU Length of Stay
Zeitfenster: From date of enrollment to the date of ICU discharge (upto 100 days or more)
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Number of days from ICU admission to ICU discharge.
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From date of enrollment to the date of ICU discharge (upto 100 days or more)
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Duration of Mechanical Ventilation
Zeitfenster: Time from enrollment to the time mechanical ventilation was stopped (upto 100 days or more)
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Total duration of mechanical ventilation during the initial hospitalization.
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Time from enrollment to the time mechanical ventilation was stopped (upto 100 days or more)
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Alex Hall, DHSc, Emory University
- Hauptermittler: Gustavo Pradilla, MD, Emory University
- Hauptermittler: Jonathan Ratcliff,, MD, MPH, Emory University
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Zerebrovaskuläre Erkrankungen
- Erkrankungen des Gehirns
- Erkrankungen des zentralen Nervensystems
- Erkrankungen des Nervensystems
- Gefäßerkrankungen
- Herz-Kreislauf-Erkrankungen
- Pathologische Prozesse
- Blutung
- Angeborene Anomalien
- Herz-Kreislauf-Anomalien
- Intrakranielle Blutungen
- Gefäßmissbildungen
- Angeborene, erbliche und neonatale Krankheiten und Anomalien
- Pathologische Zustände, Anzeichen und Symptome
- Hirnblutung
- Arteriovenöse Fehlbildungen
Andere Studien-ID-Nummern
- 2026P000373
Plan für individuelle Teilnehmerdaten (IPD)
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Beschreibung des IPD-Plans
IPD-Sharing-Zugriffskriterien
Art der unterstützenden IPD-Freigabeinformationen
- STUDIENPROTOKOLL
- SAFT
- ANALYTIC_CODE
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