Military University Hospital Prague
Prague, 16000, Czechia
Location status: Recruiting
Location contact
Martin Majovsky, MD, Ass. Prof., PhD, FEBNS
CONTACT
Norbert Svoboda, MD, PhD, FEBNS
CONTACT
++420973202932
NCT Number: NCT07614399
Dear Sir or Madam,
You have been invited to participate in a clinical study whose aim is to compare the effectiveness of two different approaches to the treatment of cerebrospinal fluid (CSF) pseudomeningocele - conservative management and interventional treatment (surgical or drainage procedures). CSF pseudomeningocele is a complication that may occur after brain surgery and is characterized by an accumulation of cerebrospinal fluid beneath the skin. At present, there is no clear consensus regarding the optimal treatment approach.
How the study will be conducted
After enrollment in the study, you will be randomly assigned (by chance) to one of two groups:
Conservative management: no surgical intervention, regular follow-up, and wound care.
Interventional treatment: simple aspiration/puncture, insertion of a lumbar drain, or reoperation.
During the study, you will be followed for a period of 1 year. Follow-up examinations will include clinical assessment and brain imaging (CT or MRI) at 4 months and 12 months after enrollment.
Risks associated with the interventional group Simple cyst aspiration/puncture: infection, bleeding into the pseudomeningocele.
Lumbar drainage: infection, meningitis, bleeding at the insertion site, cerebrospinal fluid leakage, nerve root irritation, headaches.
Reoperation: bleeding, infection, complications related to general anesthesia. Expected duration of participation in the study
12 months
Expected total number of participants enrolled in the study
20 participants
Benefit of the study
The aim of the study is to compare the effect of surgical intervention with conservative management.
Compensation for participation
Participation in this study is not associated with any financial compensation.
Interested in participating?
Request Info18 year–80 year
All sexes
Interventional
Not applicable
Prague, 16000, Czechia
Location status: Recruiting
Martin Majovsky, MD, Ass. Prof., PhD, FEBNS
CONTACT
Norbert Svoboda, MD, PhD, FEBNS
CONTACT
++420973202932
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Insertion of Lumbar drain
aspiration of the CSF fluid with injection
after aspiration of the CSF a fibrin glue is injected into the pseudomeningocele
Revision surgery in order to prevent future pseudomeninogocele formation
Time frame: 12 months
New-onset wound CSF leakage requiring revision surgery, or pseudomeningocele associated with severe headaches not responsive to analgesics.
Time frame: 12 months
To compare the infection rate between the two treatment groups.
Time frame: 12 months
To assess functional recovery using the Glasgow Outcome Scale-Extended (GOSE) at 1 year post-surgery.
Time frame: 12 months
Absorption of pseudomendingocoele at 4 months and 1 year post-surgery assessed by CT or MRI
Time frame: 12 months
Persistence of headache after the surgery - Pain Scale 0-10 (VAS)
Contact information is provided by the study sponsor or research team.
Charles University, Czech Republic
Other
Conservative Versus Interventional Management of Postsurgical CSF Pseudomeningocele: A Randomized Controlled Trial
Acronym: PSEUDO
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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