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Trial Title:
Using Polyglycolic Acid Mesh Prevents Cerebrospinal Fluid Leakage
NCT ID:
NCT06472505
Condition:
Pituitary Tumor
Cerebrospinal Fluid Leakage
Conditions: Official terms:
Pituitary Neoplasms
Pituitary Diseases
Cerebrospinal Fluid Leak
Conditions: Keywords:
Pituitary tumor
Endoscopic transnasal transsphenoidal
CSF leakage
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Device
Intervention name:
polyglycolic acid(Neoveil)
Description:
This study plans to enroll patients with pituitary tumors who need to undergo surgical
treatment according to current routine medical standards. After the tumor tissue is
removed, the integrity of the spider web or skull base will be thoroughly checked by
endoscopy during the operation to confirm whether there is any cerebrospinal fluid
leakage. At the end of the operation, use a 100*50*0.15mm, green sheet-like Navi tissue
repair patch, cut it aseptically to fit the size of the defect for repair (the common
case is 2*3.5cm defect), and place it on the spider web or skull base Tissue repair at
the surgical site to prevent cerebrospinal fluid leakage.
Arm group label:
Using polyglycolic acid mesh
Summary:
The papers propose a new method to prevent postoperative cerebrospinal fluid leakage.
Doctors use the absorbable polyglycolic acid (PGA) and fibrin glue to repair in surgery,
prevent cerebrospinal fluid leakage and reduce the necessity of postoperative lumbar
drainage after surgery. This study will analyze the changes in cerebrospinal fluid
leakage in patients with pituitary tumors and skull base tumors after surgery, and
further understand the effectiveness of Neoveil , as the basis for the development of new
treatments.
Detailed description:
Neoveil, the main component, is polyglycolic acid (PGA), which is a kind of absorbable
material, and is made into a soft and tension non-woven material by special processing
with good tissue compatibility and degradability. In the human body, its strength will
gradually decrease due to hydrolysis, and will eventually be absorbed and metabolized. In
the process of absorption, at first its strength is reduced, then the mass will gradually
decrease, and it will be completely absorbed after about 15 weeks. At present, the United
States, Europe, Australia, China and South Korea have been marketed, it is applied to the
spine , pituitary tumors , skull base tumors and aneurysm surgery,etc. inthe related
field of Neurosurgery in foreign countries. It can prevent the leakage of cerebrospinal
fluid, and reduce the postoperative hospital stay and the probability of complications
after surgery. There is a license from the TFDA. In clinical, it can be used in the
sutures of parts or fragile organs that do not need to be healed for a long time, such as
the lung, liver, and digestive tract, by suture (thick slice and tube type) or adhesion
(Sheet) In the tissue, it can strengthen the compressive ability of the local tissue,
prevent the suture thread from splitting the suture tissue, prevent the lung tissue from
leaking, reduce the blood and fluid leakage from the surgical site, and reduce the
postoperative hospital stay and after the operation The complication rate .
Criteria for eligibility:
Criteria:
A. Inclusion criteria
1. Patients with primary or recurrent pituitary tumors require endoscopic nasal
surgery.
B. Exclusion criteria
1. Patients with pituitary gland tumors who do not receive surgical treatment.
2. Patients with other brain tumors.
3. Patients allergic to polyglycolic acid (PGA).
4. Patients who have had previous radiation therapy or chemotherapy.
Gender:
All
Minimum age:
20 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
National Taiwan University Hospital
Address:
City:
Taipei
Zip:
100
Country:
Taiwan
Status:
Recruiting
Contact:
Last name:
Abel Huang, MD
Phone:
+8860223123456
Phone ext:
265913
Email:
how.how0622@gmail.com
Start date:
December 1, 2023
Completion date:
December 31, 2025
Lead sponsor:
Agency:
National Taiwan University Hospital
Agency class:
Other
Source:
National Taiwan University Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06472505