Reduction of Edema With a Specialized Cocktail for Ultra-early Management in Intracerebral Hemorrhage

Last updated: May 11, 2025
Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University
Overall Status: Active - Not Recruiting

Phase

3

Condition

Brain Injury

Stroke

Hemorrhage

Treatment

PPA Intervention

Clinical Study ID

NCT06863558
RESCUE-ICH
  • Ages > 18
  • All Genders

Study Summary

Intracerebral hemorrhage (ICH) is a severe stroke subtype with high mortality and disability rates, often worsened by perihematomal edema (PHE), which increases intracranial pressure and leads to poor outcomes. Preclinical studies suggest that a pharmacological cocktail (PPA) may help reduce cerebral edema by modulating potassium balance, preserving aquaporin-4 expression, and enhancing lymphatic drainage.

This multicenter, randomized controlled trial (RCT) aims to evaluate the safety and efficacy of PPA in ICH patients. A total of 58 patients with supratentorial ICH (≥3 mL hematoma volume) who are not undergoing surgical evacuation will be randomized to receive either PPA therapy or standard treatment. The primary outcome is the change in cerebral edema volume at 5-7 days, assessed by CT imaging. Secondary outcomes include 90-day functional outcomes (mRS), need for decompressive craniectomy, and safety assessments. This study seeks to explore PPA as a potential treatment strategy for cerebral edema in ICH patients.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age ≥18 years

  • Clinical diagnosis of supratentorial intracerebral hemorrhage (ICH)

  • Symptom onset within 3 days (≤72 hours) before randomization

  • Baseline CT-confirmed hematoma volume ≥3 mL

  • Not scheduled for hematoma evacuation surgery (either not indicated or declined bythe patient/family)

  • Written informed consent obtained from the patient or legally authorizedrepresentative

Exclusion

Exclusion Criteria:

  • Baseline brain herniation or severe hypotension (SBP <90 mmHg)

  • Contraindications to PPA medications (terazosin, urapidil, esmolol, propranolol),such as asthma or severe bradycardia

  • Severe comorbidities that may interfere with efficacy assessment or pose a highsafety risk (e.g., end-stage organ failure, advanced malignancy)

  • Presence of secondary causes of ICH (e.g., arteriovenous malformation, aneurysmrupture, hemorrhagic transformation of ischemic stroke)

  • Pregnancy or lactation

  • Participation in another interventional trial that may influence study outcomes

Study Design

Total Participants: 58
Treatment Group(s): 1
Primary Treatment: PPA Intervention
Phase: 3
Study Start date:
May 08, 2025
Estimated Completion Date:
June 30, 2026

Study Description

Intracerebral hemorrhage (ICH) is a severe subtype of stroke, accounting for 15-20% of all strokes. Compared to ischemic stroke, ICH has a higher mortality and disability rate, with its incidence steadily rising worldwide, imposing a substantial burden on families and healthcare systems. A key factor contributing to poor prognosis in ICH is perihematomal edema (PHE), which rapidly progresses during the acute phase, leading to increased intracranial pressure (ICP), brain tissue displacement, and potential brain herniation. Even in patients who survive the acute phase, persistent cerebral edema can cause long-term neurological deficits and impair quality of life. Therefore, effective management of cerebral edema is critical for improving outcomes in ICH patients.

Preclinical studies suggest that a pharmacological cocktail (PPA), consisting of adrenergic antagonists, may help reduce cerebral edema by modulating extracellular potassium homeostasis, maintaining aquaporin-4 (AQP-4) expression, and enhancing lymphatic drainage. In both traumatic brain injury and ischemic stroke models, PPA has shown potential in alleviating cerebral edema and improving neurological recovery. Based on these findings, this multicenter, randomized controlled trial (RCT) aims to evaluate the safety and efficacy of PPA in reducing cerebral edema in ICH patients.

The study will enroll 58 patients diagnosed with supratentorial ICH (≥3 mL hematoma volume) who are not undergoing surgical evacuation. Participants will be randomly assigned to receive PPA therapy or standard treatment. The primary outcome is change in cerebral edema volume at 5-7 days, assessed by CT imaging. Secondary outcomes include functional outcomes at 90 days (mRS), need for decompressive craniectomy, incidence of hypotension, and adverse events. This study aims to explore PPA as a novel pharmacological approach for managing cerebral edema in ICH, potentially improving patient prognosis and clinical outcomes.