Safety Study of Minimally Invasive Approaches to Unruptured Anterior Circulation Aneurysms

Not Applicable

• Conditions: Aneurysm, Middle Cerebral Artery; Aneurysm, Posterior Communicating Artery; Brain Aneurysm; Aneurysm, Anterior Communicating Artery; Cerebral Aneurysm; Aneurysm, Carotid Artery
• Interventions: Procedure: Aneurysm Clipping

• Registration Number: NCT02345395
• Lead Sponsor: University of Sao Paulo General Hospital

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.

Study Timeline

• Study Start: 2013-09
• Status Verified: 2014-01
• Study First Submitted: 2015-01-19
• Study First Submitted QC: 2015-01-23
• Last Update Submitted: 2015-01-23
• Study First Posted: 2015-01-26
• Last Update Posted: 2015-01-26
• Primary Completion: 2015-07
• Study Completion: 2015-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 120

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)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Transpalpebral Approach	Aneurysm Clipping	Aneurysm Clipping - Patients will be submitted to a Transpalpebral Approach to Unruptured Anterior Circulation Aneurysm and they will be discharged from the hospital on the next day.
Classical Pterional Craniotomy	Aneurysm Clipping	Aneurysm Clipping - Patients will be submitted to a Classical Pterional Approach to Unruptured Anterior Circulation Aneurysm and they will be discharged from the hospital 4-5 days after the procedure.
NanoPterional Approach	Aneurysm Clipping	Aneurysm Clipping - Patients will be submitted to a Modified MiniPterional Approach (Nanopterional) to Unruptured Anterior Circulation Aneurysm and they will be discharged from the hospital on the next day.

Primary Outcome Measures

Name	Time	Method
Effective Aneurysm Clipping (no residual cerebral aneurysm)	3 months after surgery	All patients will be submitted to a post operative angiography to asses the presence of residual cerebral aneurysm after clipping.

Secondary Outcome Measures

Name	Time	Method
All Cause Mortality	1 year
Neurological Outcome	1 year	All patients will be classified with the Glasgow Outcome Scale, Rankin Scale
Cosmetic Outcome	1 year	Comparison of pre and post operative photos and asses of patients satisfaction
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 Discharge	15 days	Safety of early Discharge in the Experimental Groups (need of early hospital readmission? and its causes)

Trial Locations

Locations (1)

Hospital das Clínicas of University of São Paulo Medical School; 🇧🇷 Sao Paulo, Brazil