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A Clinical Trial About the Safety of Surgical Treatment in Severe Primary Pontine Hemorrhage

Not Applicable
Recruiting
Conditions
Cerebrovascular Disorders
Pontine Hemorrhage
Primary
Surgery
Interventions
Other: life support
Procedure: hematoma evacuation by craniotomy
Procedure: hematoma evacuation by stereotactic puncture
Procedure: hematoma evacuation by neuroendoscopy
Registration Number
NCT04647162
Lead Sponsor
West China Hospital
Brief Summary

Primary pontine hemorrhage (PPH) is not common but is the most catastrophic subtype of intracerebral hemorrhage, with acute mortality between 30% and 60%. For severe PPH, defined as Glasgow Coma score (GCS) \<8 and hematoma volume≥5ml, the mortality rate is as high as 80-100%. Guidelines from the American Heart Association and European Stroke Organization do not make definite specifications. More than a century after Finkelnburg first explored the brainstem for hematoma, however, plenty of researches have shown surgery can save lives and improve the prognosis for selective patients and can be an effective and safe treatment. This study is proposed to validate the safety of surgical treatment in severe primary pontine hemorrhage.

Detailed Description

The study is being conducted from Jan 2022 to Nov 2024 in 20 neurosurgical units. This STIPE trial is an investigator-initiated, parallel (3:1 to surgical HE or MT), multi-centre, randomized controlled open-label trial following the Consolidated Standards of Reporting Trials (CONSORT) guidelines and will be conducted from Jan 2022 to Nov 2024 in 20 Tertiary hospitals in China. The flow chart of the clinical trial is presented in Figure 1. Neurosurgeons involved in the study are senior investigators with good clinical experience in sPPH management. Moreover, all investigators are well trained centrally according to the requirements.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
64
Inclusion Criteria
  1. Clinical diagnosis of PPH: patients have acute hemorrhage mainly in pons with a definite history of hypertension.
  2. GCS 5~7 and HV≥5ml on admission (the HV in intraventricular system being excluded).
  3. Family members consenting to randomize and signing informed consent form (ICF).
  4. Time from onset to admission less than 24 hours.
  5. Age:18 years or older.
Exclusion Criteria
  1. Structural lesions such as brainstem cavernous malformation, arteriovenous malformation, aneurysm, tumor apoplexy.
  2. GCS≥8 and HV<5ml.
  3. Time from onset to admission over 24 hours.
  4. Patients with platelet count < 100,000, International Normalized Ratio (INR)> 1.4, or an elevated prothrombin time (PT) and activated partial thromboplastin time (APTT).
  5. Multiple ICH.
  6. Accompanying hydrocephalus that requires surgical management
  7. Irreversible brainstem failure (bilateral fixed, dilated pupils and extensor motor posturing, GCS≤4).
  8. A previous history of ICH.
  9. Any serious concurrent illness that would interfere with the safety assessments including hepatic, renal, gastroenterologic, respiratory, cardiovascular, endocrinologic, immunologic, and hematologic disease.
  10. Pregnant patients.
  11. Patients' family members refuse HE.
  12. Any other condition that the investigator believes would present a significant hazard to the subject if the investigational therapy were initiated.
  13. Participating in another simultaneous trial of ICH treatment.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
surgical grouphematoma evacuation by neuroendoscopyPatients receive intervention such as the evacuation of hematoma under craniotomy or by stereotactic puncture or neuroendoscopy.
medical grouplife supportPatients receive only medical treatment including active life support, nutritional support, homeostasis maintenance of the internal environment, and other symptomatic treatment.
surgical grouphematoma evacuation by craniotomyPatients receive intervention such as the evacuation of hematoma under craniotomy or by stereotactic puncture or neuroendoscopy.
surgical grouphematoma evacuation by stereotactic puncturePatients receive intervention such as the evacuation of hematoma under craniotomy or by stereotactic puncture or neuroendoscopy.
Primary Outcome Measures
NameTimeMethod
Safety Outcome Number 3: Rate of Symptomatic Rebleeding72 hours post surgery

The difference in the rate of symptomatic rebleeding 72 hours post surgery.

Safety Outcome Number 1: Rate of Mortality30 days from randomization

Percentage of participants who died during the first 30 days after randomization.

Safety Outcome Number 2: Rate of Cerebritis, Meningitis, Bacterial Ventriculitis30 days from randomization

Percentage of participants who had a bacterial brain infection (cerebritis, meningitis, ventriculitis) within 30 days of randomization.

Secondary Outcome Measures
NameTimeMethod
neurological functional status of 30 days, 90 days, 180 days, and 365 days measured by Modified Rankin Scale (mRS), GCS and GOS.30 days, 90 days, 180 days, and 365 days after surgery

neurological functional status of 30 days, 90 days, 180 days, and 365 days measured by Modified Rankin Scale (mRS), GCS and GOS.

The Extended Glasgow Outcome Scale (EGOS) at 180 days and 365 days180 days and 365 days after surgery

The Extended Glasgow Outcome Scale (EGOS) at 180 days and 365 days

the rate of hematoma clearance 3 days after surgery3 days after surgery

the rate of hematoma clearance 3 days after surgery

all-cause mortality at 365 days365 days after surgery

all-cause mortality at 365 days

The 5-level EuroQol five dimensions questionnaire (EQ-5D) version (EQ-5D-5L) at 180 days and 365 days180 days and 365 days after surgery

The EQ-5D-5L essentially consists of 2 pages: the EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS). The former descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state. The latter is numbered from 0 to 100. 100 means the best health you can imagine. 0 means the worst health you can imagine.

the National Institutes of Health Stroke Scale (NIHSS) at 180 days and 365 days180 days and 365 days after surgery

the National Institutes of Health Stroke Scale (NIHSS) at 180 days and 365 days

Trial Locations

Locations (20)

The Second Affiliated Hospital of Zhengzhou University

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Zhengzhou, Henan, China

Xuhui Hospital of Zhongshan Hospital affiliated to Fudan

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Shanghai, China

The First Affiliated Hospital of Anhui Medical University

🇨🇳

Hefei, Anhui, China

The First Affiliated Hospital of Fujian Medical University

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Fuzhou, Fujian, China

Gaozhou Hospital of Traditional Chinese Medicine Affiliated to Guangzhou University of Chinese Medicine

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Gaozhou, Guangdong, China

The Second Affiliated Hospital of South China University of Technology

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Shenzhen, Guangdong, China

Zhuhai People's Hospital

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Zhuhai, Guangdong, China

The First Affiliated Hospital of Harbin Medical University

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Harbin, Heilongjiang, China

Shanxi Bethune hospital

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Taiyuan, Shanxi, China

West China Hospital of Sichuan University

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Chengdu, Sichuan, China

Mianyang Central Hospital

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Mianyang, Sichuan, China

Affiliated Hospital of North Sichuan Medical College

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Nanchong, Sichuan, China

The Third Hospital of the People's Liberation Army

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Baoji, China

The seventh medical center of the Army General Hospital

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Beijing, China

Second Affiliated Hospital of Zhejiang University School of Medicine

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Hangzhou, China

Huashan Hospital of Fudan University

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Shanghai, China

Shanghai No.10 hospital

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Shanghai, China

Guangdong Sanjiu Brain Hospital

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Guangzhou, Guangdong, China

University of Chinese Academy of Sciences Shenzhen Hospital

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Shenzhen, Guangdong, China

General Hospital of the Eastern Theater

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Nanjing, Jiangsu, China

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