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Safety Study of Minimally Invasive Approaches to Unruptured Anterior Circulation Aneurysms

Safety Study of Minimally Invasive Approaches to Unruptured Anterior Circulation Aneurysms

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02345395
Acronym
MININCRUSP
Enrollment
120
Registered
2015-01-26
Start date
2013-09-30
Completion date
2015-12-31
Last updated
2015-01-26

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

Conditions

Aneurysm, Anterior Communicating Artery, Aneurysm, Carotid Artery, Aneurysm, Middle Cerebral Artery, Aneurysm, Posterior Communicating Artery, Brain Aneurysm, Cerebral Aneurysm

Keywords

Brain Aneurysm, Pterional Craniotomy, MiniPterional Craniotomy, Transpalpebral Approach, Unruptured Brain Aneurysm

Brief summary

The study is designed to evaluate the efficacy and safety of minimally invasive neurosurgical techniques for patients with incidental cerebral aneurysms of the anterior circulation in the Hospital das Clínicas of the University of São Paulo Medical School.

Detailed description

Minimally Invasive Neurosurgery is a inexorable tendency and it is already a reality in many centers of the world. It is a broad and relative concept and there is few consistent medical data to validate its benefits. In this manner, this is the first clinical trial in Brazil questioning the safety of the of minimally invasive surgery to treat incidental cerebral aneurysms of the anterior circulation. For countries like Brazil, the indirect demonstration of reduction in hospital costs through lower hospital stays is a breakthrough to provide better health for the entire population. Patients with the diagnosis of incidental brain aneurysms of the anterior circulation will be recruited from the spontaneous demand of the Hospital das Clínicas of University of São Paulo Medical School. The investigators expect to recruit 60 patients for the experimental group and 60 for the control group. In the study group patients will be submitted to a minimally invasive approach (transpalpebral mini fronto-orbital craniotomy or modified minipterional craniotomy). All patients in this group will be submitted to surgery starting at 8 o'clock in the morning. After 6 hours of the end of surgery, all patients will have a control CT scan and if the result is adequate, they are going to be discharged from the ICU with no IV drugs. The hospital discharge will be in the next day. The control group are patients that will be submitted to a classical pterional craniotomy with hospital discharge occurring in 4-5 days. All patients will be submitted to the standard care offered by the Hospital das Clinicas. All surgical and ambulatory data will be collected by the main investigators (Dr. Mauricio Mandel and Dr. Eberval Figueiredo). The adverse events will be promptly reported to the chair of the department and to the CAPPESQ (the ethics committee of the hospital). Ambulatory data will be collected during the regular post operative medical appointments and a web based questionnaire. The post operative follow-up is unified in only one ambulatory center and day (thursdays mornings). Statistical analysis will compare primary and secondary objectives of the two groups, as specified in the study protocol.

Interventions

All Patients will be submitted to a surgical intervention in order to clip their unruptured brain aneurysm

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with the diagnosis of incidental unruptured cerebral aneurysms (4mm to 2cm)

Exclusion criteria

* Patients who do not have adequate family care during the immediate post-operative period (the patient's family must commit to stay with the patient in the first five days after hospital discharge) * Patients who are unable to communicate by telephone * People with cardiovascular disease, liver or kidney failure. * Pregnant women or breastfeeding * Patients with coagulation abnormalities * Patients with High Surgical Risk evaluated by different risk scores (ASA, AHA, Goldman, Detsky)

Design outcomes

Primary

MeasureTime frameDescription
Effective Aneurysm Clipping (no residual cerebral aneurysm)3 months after surgeryAll patients will be submitted to a post operative angiography to asses the presence of residual cerebral aneurysm after clipping.

Secondary

MeasureTime frameDescription
All Cause Mortality1 year
Neurological Outcome1 yearAll patients will be classified with the Glasgow Outcome Scale, Rankin Scale
Surgical Safety assessed by number and description of Surgical Complications (infection rate, postoperative epidural/ contusional hematomas, number of reoperations, need of blood transfusion)1 year
Early Hospital Discharge15 daysSafety of early Discharge in the Experimental Groups (need of early hospital readmission? and its causes)
Cosmetic Outcome1 yearComparison of pre and post operative photos and asses of patients satisfaction

Other

MeasureTime frameDescription
Quality of Life15 days, 3 months, 6 months and 1 yearWhoqol-bref questionnaire

Countries

Brazil

Contacts

Primary ContactMauricio Mandel, MD
mauricio.mandel@gmail.com55 11 996299224
Backup ContactEster M Tomazini
ester.t@hc.fm.usp.br55 11 2661-7152/8014

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026