Cerebral, Meningeal Biopsy by Flexible Endoscopy in Patients Without Neurological Diagnosis
1 other identifier
observational
40
1 country
1
Brief Summary
The investigators will take cerebral and subarachnoid biopsy by flexible endoscopy in patients without neurological findings. The investigators will use retrospective and prospective patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Nov 2009
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2010
CompletedFirst Submitted
Initial submission to the registry
February 22, 2010
CompletedFirst Posted
Study publicly available on registry
February 23, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2010
CompletedFebruary 23, 2010
February 1, 2010
2 months
February 22, 2010
February 22, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Test the useful of the cerebral and subarachnoid biopsy by flexible endoscopy in patients without neurological findings
2 weeks
Secondary Outcomes (1)
Developed a diagnosis method for idiopathic neurological findings. Compare the cerebral and subarachnoid biopsy each other
2 weeks
Study Arms (1)
undeterminated neurological disease, cerebral endoscopy
patients without neurological diagnosis that require cerebral , meningeal diagnosis
Interventions
The investigators will make a burrhole in the precoronal suture introducing the flexible endoscope taking a cerebral and a basal meningeal biopsy
Eligibility Criteria
Patients between 0 and 85years old with neurological diseases that there are not a diagnosis
You may qualify if:
- patients with neurological disease and with out diagnosis
You may not qualify if:
- death of the patient
- patients with neurological diagnosis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hospital Central Dr. Ignacio Morones Prieto
San Luis Potosí City, San Luis Potosí, 78210, Mexico
MeSH Terms
Conditions
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
February 22, 2010
First Posted
February 23, 2010
Study Start
November 1, 2009
Primary Completion
January 1, 2010
Study Completion
October 1, 2010
Last Updated
February 23, 2010
Record last verified: 2010-02