Actively Recruiting

Age: 18Years +
All Genders
ID06724029

Neurosurgical Outcome Network for Predicting Outcomes in Neurosurgery

Led by Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta · Updated on 2026-03-30

4500

Participants Needed

27

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating outcomes and their predictors in various neurosurgical conditions to improve the quality and consistency of research and clinical care. The study focuses on standardizing the assessment of clinical, cognitive, and psychological status before and after neurosurgical interventions across multiple centers. This effort aims to create a common language in routine practice and support better therapeutic decisions through shared data and identified predictive factors. The study collects detailed clinical and demographic information from patients undergoing neurosurgery for a wide range of conditions, including tumors, vascular diseases, trauma, spinal disorders, functional pathologies, peripheral nerve issues, and malformations. Data such as comorbidities, anesthesia details, complications, and psychological assessments are gathered before surgery and at follow-ups, with timing varying by condition. An artificial intelligence analysis will be used to identify important predictors and outcomes. Participants will provide data over a period of up to five years, including sociodemographic details, clinical status, cognitive and psychological assessments, and complication records. The study monitors these factors preoperatively and postoperatively to describe outcomes and explore associations with preoperative indicators. The long-term collection of data supports understanding neurosurgical results and guiding patient care more precisely.

CONDITIONS

Brief Title

Neurosurgical Outcome Network

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Diagnosis of neuro-oncological tumors excluding skull base tumors
  • Presence of basicranial tumors from anterior, middle, or posterior cranial fossae or sellar regions
  • Vascular pathologies including aneurysms, arteriovenous malformations, cavernomas, Moyamoya disease, dural fistulas, or nontraumatic hematomas
  • Traumatic brain injuries such as diffuse damage, subdural or extradural hematomas, subarachnoid hemorrhage, intraparenchymal hematoma, fractures, or hydrocephalus
  • Spinal pathologies including degenerative, myelopathic, traumatic, and oncologic conditions
  • Functional disorders like Parkinson's disease, spasticity, trigeminal neuralgia, craniofacial pain, neuropathic pain, tremor, dystonias, obsessive-compulsive disorder, drug-resistant epilepsy, depression, or normotensive hydrocephalus
  • Peripheral nervous system conditions including nerve compression syndromes, tumors, and trauma
  • Malformative conditions such as Chiari malformation type 1, craniostenoses, and malformative hydrocephalus
  • Adequate understanding of Italian language
  • Diagnosis of glioma, meningioma, vascular pathology, or spinal pathology to qualify for cognitive and psychological assessment
Not Eligible

You will not qualify if you...

  • History of psychiatric diseases or current use of psychotropic drugs for cognitive and psychological assessments
  • Presence of overt cognitive decline not caused by neurosurgical injury
  • Age younger than 18 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 1 year

Participants undergo collection of preoperative clinical, cognitive, and psychological data related to their neurosurgical pathology.

Visits as scheduled before surgery depending on pathology

Surgery and Immediate Post-operative Care

Duration - Variable based on intervention and hospitalization

Participants undergo neurosurgical intervention and immediate postoperative clinical care with collection of relevant clinical data.

Hospital visits during intervention and immediate recovery period

Post-operative Follow-up

Duration - Up to 5 years

Participants have follow-up visits to collect postoperative clinical, cognitive, and psychological data to evaluate outcomes and predictors.

Regular follow-up visits scheduled over 5 years depending on pathology

Trial Site Locations

Total: 27 locations

1

1. ASST Papa Giovanni XXIII

Bergamo, BG, Italy, 24127

Active, Not Recruiting

2

Spedali Civili Brescia

Brescia, BS, Italy, 25123

Active, Not Recruiting

3

Fondazione Poliambulanza Istituto Ospedaliero

Brescia, BS, Italy, 25124

Active, Not Recruiting

4

Ospedale Moriggia Pelascini

Gravedona, Como, Italy, 22015

Active, Not Recruiting

5

ASST Lariana, Ospedale S. Anna

Como, CO, Italy, 22100

Active, Not Recruiting

6

ASST Cremona

Cremona, CR, Italy, 26100

Active, Not Recruiting

7

Fondazione IRCCS San Gerardo dei Tintori

Monza, MB, Italy, 20900

Active, Not Recruiting

8

Fondazione IRCCS Policlinico San Matteo

Pavia, PV, Italy, 27100

Active, Not Recruiting

9

ASST della Valtellina ed Alto Lario

Sondrio, SO, Italy, 23100

Active, Not Recruiting

10

Azienda Ospedaliero Universitaria Policlinico "G. Rodolico - San Marco"

Catania, Italy

Actively Recruiting

11

Azienda Ospedaliero Universitaria Careggi

Florence, Italy

Actively Recruiting

12

Ospedale F. Spaziani di Frosinone

Frosinone, Italy, 03100

Actively Recruiting

13

Ospedale Alessandro Manzoni

Lecco, Italy, 23900

Active, Not Recruiting

14

ASST Ovest Milanese

Legnano, Italy, 20025

Active, Not Recruiting

15

Ospedali Riuniti di Livorno -Azienda USL Toscana nord ovest

Livorno, Italy

Actively Recruiting

16

Fondazione IRCCS Istituto Neurologico Carlo Besta

Milan, Italy, 20133

Actively Recruiting

17

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Milan, Italy, 20122

Active, Not Recruiting

18

ASST Santi Paolo e Carlo

Milan, Italy, 20153

Actively Recruiting

19

ASST Fatebenefratelli Sacco

Milan, Italy

Active, Not Recruiting

20

Istituto Clinico Città Studi

Milan, Italy

Active, Not Recruiting

21

Policlinico di Monza

Monza, Italy, 20900

Actively Recruiting

22

A.R.N.A.S. Ospedali Civico di Palermo

Palermo, Italy, 90127

Actively Recruiting

23

Azienda Ospedaliero Universitaria di Parma

Parma, Italy

Active, Not Recruiting

24

ASL Roma 1

Roma, Italy, 00135

Actively Recruiting

25

Fondazione Policlinico Universitario Gemelli di Roma

Roma, Italy, 00168

Actively Recruiting

26

IRCCS Istituto Clinico Humanitas

Rozzano, Italy, 20089

Active, Not Recruiting

27

Azienda Sanitaria Universitaria Friuli Centrale di Udine

Udine, Italy, 33100

Actively Recruiting

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Research Team

P

Paolo Ferroli, MD

M

Morgan A Broggi, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Accuracy of operating neurosurgeons' prediction of functional levels after intracranial tumor surgery.

Lisa Millgård Sagberg, Christina Drewes, Asgeir S Jakola...

https://pubmed.ncbi.nlm.nih.gov/27315026

Evidence for the use of preoperative risk assessment scores in elective cranial neurosurgery: a systematic review of the literature.

Elina Reponen, Hanna Tuominen, Miikka Korja

https://pubmed.ncbi.nlm.nih.gov/25046789