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Comparison Between Stereotactic Aspiration and Intra-endoscopic Surgery to Treat Intracerebral Hemorrhage

Comparison Between Stereotactic Aspiration and Intra-endoscopic Surgery to Treat Intracerebral Hemorrhage

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02515903
Acronym
EndoSurofICH
Enrollment
100
Registered
2015-08-05
Start date
2015-05-31
Completion date
2016-11-30
Last updated
2015-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intracerebral Hemorrhage, Surgery

Keywords

Endoscopy, Intracerebral hemorrhage, surgery, stereotactic aspiration, Key-hole approach, Intracerebral hemorrhage surgical treatment, Transparent endoscopic sheath, Agitation-aspiration device

Brief summary

Views for surgery method selection of intracerebral hemorrhage are still controversial. Since the application of neuroendoscopic technique in intraventricular hemorrhage was confirmed effective and safe, some investigators have attempted to use endoscopic strategies to evacuate intracerebral hematomas. Some significant advances have also been reported in endoscopic hematoma evacuation when compared to conventional craniotomy. However, it is still crucial to implement a prospective and controlled study to evaluate the efficiency and safety of endoscopic technique in the treatment of intracerebral hemorrhage. In this study, the investigators will exclusively select some patients with intracerebral hemorrhage in the basal ganglia region. This study will compare the efficacy and safety of endoscopic surgery versus stereotactic aspiration on neurologic outcomes for patients with intracerebral hemorrhage.

Detailed description

Although the incidence and mortality of spontaneous intracerebral hemorrhage (ICH) have been decreased with the improved management of high blood pressure, ICH may induce serious disability for the patients and continue to be a major socioeconomic problem. The evacuation of ICH using open craniotomy or computer tomography (CT)-guided stereotaxy may improve the survival rate of these patients but failed to prove efficacy in improving patients' functional outcome despite numerous efforts. Endoscopy-guided evacuation of ICH provides a less invasive and quicker surgical decompression, which may potentially improve the functional outcome for patients. In previous studies, endoscope-guided evacuation of ICH is often referred to as that an endoscope only provides an illuminating system while the operating channel is independent from the endoscope (endoscopy-controlled microneurosurgery or endoscopy-assisted microneurosurgery). In recent years, authors have been committed to explore the procedure of intra-endoscopy-guided evacuation of ICH, which means that the illuminating channel, the irrigation-aspiration channel and the working channel are all located in the endoscope. This kind of procedure can be called as real endoscopic neurosurgery (EN), which may potentially decrease the operative concomitant injuries at the most extent. However, the inherent drawbacks of intra-endoscopic procedures, including the limited visualization of the surgical field and the difficult maintenance of patency of the aspiration wand, can offset the advantages in some instances. The authors exclusively invented a special endoscopic transparent sheath for guiding hematoma puncture and an agitation-aspiration system (AAS) for keeping patency of the aspiration wand. Detailed procedures of their application will be implemented and verified in a series of patients with intracerebral hemorrhage. Meanwhile, the mortality rate, complications and other outcome parameters between this procedure and CT-guided procedures will be compared.

Interventions

PROCEDUREIntra-endoscopic surgery

Intra-endoscopic surgery for evacuation of ICH

PROCEDUREPlacebo:stereotactic aspiration surgery

Placebo:stereotactic aspiration surgery for evacuation of ICH

Sponsors

Shenzhen People's Hospital
CollaboratorOTHER
Nanfang Hospital, Southern Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* primary basal ganglion region intracerebral hemorrhage * older than 18 years * admitted within 6 h after onset of ICH

Exclusion criteria

* other type of ICH than acute primary intracerebral hemorrhage * patients who need neurosurgery * life expectancy less than 3 months due to comorbid disorders * confirmed malignant disease (cancer) * confirmed acute myocardial infarction * hepatitis and/liver cirrhosis * renal failure * infectious disease (HIV, endocarditis etc.) * current or previous hematologic disease * women of childbearing age if pregnant * participation in another study within the preceding 30 days

Design outcomes

Primary

MeasureTime frameDescription
Mortality rate90-dayall-cause motality rate within 90 days after the surgery

Secondary

MeasureTime frameDescription
days of ICU stay14 daythe period between the end of the surgery to leaving the ICU
remnant blood in the hematoma after surgery12 hourthis parameter will be monitored by CT scan immediately after the surgery
Glasgow coma score28 daythe GCS will be evaluated by a senior doctor 28 days after the surgery
operative time24 hthe period from skin incision to wound suture
In-hospital cost28 dayall medical cost during the in-hospital period
rehemorrhage rate3 dayRehemorrhage almost occurs within 3 days after the surger. So cranial CT scan will be performed routinely 3 days later after surgery to evaluate the rehemorrhage rate
intracranial infection14 dayIf the patient underwent a period of fever, cerebral fluid will be withdrawn by means of lumbar puncture and tested to verify whether the intracranial infection occurs
Glasgow outcome score90-daythe GCS will be evaluated by a senior doctor 28 days after the surgery

Countries

China

Contacts

Primary ContactBo Du, MD
ftipa@163.com86-13823699011
Backup ContactYu-ping Peng, MD
83936462@qq.com86-15914141979

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026