Chitosan Scaffold for Sellar Floor Repair in Endoscopic Endonasal Transsphenoidal Surgery
Primary Purpose
Csf Leakage
Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Implant of bilaminar chitosan scaffold
Sponsored by
About this trial
This is an interventional treatment trial for Csf Leakage focused on measuring chitosan, endoscopic, sellar tumor, biomaterials, transphenoidal
Eligibility Criteria
Inclusion Criteria:
- male/female patient candidate for an endoscopic endonasal transphenoidal surgery, who need repair of the sellar floor as part of the surgical procedure.
Exclusion Criteria:
- Diabetes, heart diseases, immunological diseases, infectious diseases, bone diseases.
Sites / Locations
- Departamento de neurociencias
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Patient with bilaminar chitosan implant
Arm Description
A 65 year old woman, right handed, started with progressive bilateral visual loss in her temporal field, over 10 months, she underwent an MRI and it was found a sellar lesion that compressed the optic chiasm, an endoscopic endonasal transsphenoidal surgery was done for the resection of the lesion, using a novel bilaminar chitosan scaffold to assist the closure of the sellar floor.
Outcomes
Primary Outcome Measures
Brain MRI with and without contrast
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the preoperative tumor size
Brain MRI with and without contrast
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor size
Head CT scan
Bone window was used to see the repair of bone defect after surgery
Brain MRI with and without contrast
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Brain MRI with and without contrast
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Brain MRI with and without contrast
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Brain MRI with and without contrast
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Head CT scan
Bone window was used to see the repair of bone defect after surgery
Head CT scan
Bone window was used to see the repair of bone defect after surgery
Head CT scan
Bone window was used to see the repair of bone defect after surgery
Secondary Outcome Measures
Visual field test
visual field testing looking for compression of optic chiasm
Snellen test
visual acuity testing
Glasgow scale
level of consciousness
Endocrinological panel
evaluation of hipofisary function
Blood cell count
For evaluation of any inflammatory reaction or infection before or after the procedure
acute phase reactans
For evaluation of any inflammatory reaction or infection before or after the procedure
blood electrolytesand
evaluation of renal function and as requirement for surgery
liver function test
evaluation of liver function and as requirement for surgery
coagulation test
secondary evaluation of liver function, inflammatory reaction or infection before and after the procedure and as requirement for surgery.
seric creatinine
evaluation of renal function and as requirement for surgery
Full Information
NCT ID
NCT03280849
First Posted
September 4, 2017
Last Updated
March 12, 2019
Sponsor
University of Guadalajara
1. Study Identification
Unique Protocol Identification Number
NCT03280849
Brief Title
Chitosan Scaffold for Sellar Floor Repair in Endoscopic Endonasal Transsphenoidal Surgery
Official Title
Chitosan Scaffold for Sellar Floor Repair in Endoscopic Endonasal Transsphenoidal Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
January 2015 (Actual)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
February 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Guadalajara
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A 65 year old female participant , right handed, started with progressive bilateral visual loss in her temporal field, over 10 months, the participant underwent an MRI and it was found a sellar lesion that compressed the optic chiasm, an endoscopic endonasal transsphenoidal surgery was done for the resection of the lesion, using a novel bilaminar chitosan scaffold to assist the closure of the sellar floor. After a follow up of 2 years the participant returned to its normal visual function, without evidence of the sellar lesion on the postoperative MRI, and without complications.
Detailed Description
Introduction This case describe the use of a novel bilaminar chitosan scaffold in the repair of the sellar floor after an endoscopic endonasal transsphenoidal surgery for a suspected hipofisary macroadenoma, the use of chitosan as a scaffold has been described in several preclinical studies and tested in tissue bioengineering of bone, neural tissue and soft tissue, in the case of bone tissue, several studies demonstrated its potential due to its biocompatibility, osteinductive and osteoconductive features, but there is a lack of clinical trials demonstrating this characteristics in the clinical setting. One of the most common complications for the neurosurgeons after an endoscopic endonasal transsphenoidal surgery is the CSF leak, depending on the technique and the reconstruction used for the sellar floor this complication could be presented from 5% to 75%of the cases, leading to complications such infections and pneumoencephalus, representing a great risk for comorbidities, longer recovery times and hospital costs, due to this challenges in the repair of the sellar floor,the investigators intent to approach the problematic with a chitosan scaffold for its characteristics in bone regeneration. The setting of a bioactive membrane in the defect of the surgery could be useful for a stronger and more suitable closure of the sellar floor.
Case description A 65 years old female participant, right handed, came to the neurosurgery consultation with progressive bilateral visual loss in her temporal fields, with predominance in the left eye over 10 months, two weeks before her admission the participant reported a sudden loss of consciousness, prompting her to go to the hospital. In her clinical examination, the participant was alert and oriented x3, normal cranial nerves examination except for decrease visual acuity by 20/200 in her left eye, 20/80 in her right eye, bitemporal hemianopia and mild primary athropy of the optic disc in the left eye, the gait and the motor and sensitive examination was normal. The laboratory studies showed a LH: 0.22 and prolactine: 53.7 .In the contrasted preoperative brain MRI, it was found a sellar lesion, hypointense in T1 but hyperintense in T2 signal with enhancing of the periphery after the infusion of gadolinium, the lesion presented extension to the sphenoid sinus, paraselar space without involvement of the carotids and supraselar with displacement of the optic chiasm. The participant underwent endoscopic endonasal transsphenoidal surgery for resection of the sellar lesion, under the direct visualization, the lesion appeared redish and soft with moderately bleeding, a sample was taken for pathology and the remaining is extracted without complications, then the scaffold is implanted in the site of the bone defect in the sphenoid sinus, due to its moldable nature, it was easily set, covering the entire extension of the defect, a fat graft was set in the sphenoid sinus covering the bilaminar chitosan membrane, then fibrin sealant was used for hemostatic control and a nasal packing was set in both nostrils for finalize the procedure. In the postoperative there was not complication and after a few days the participant was discharged with notable clinical improvement, after one month of follow up the participant recovered her visual acuity and the participant did not refer any symptom, the participant underwent a post operative brain MRI, where it is observed a gross total resection and good closure of the sellar floor, without signs of rejection or inflammation in the zone with the chitosan scaffold.
Materials and methods for the bilaminar chitosan scaffold The bilaminar implant is constitute by two types of different structures, one of the membranes presents a flat-smooth structure, the other membrane has a tridimensional-porous structure, each of the physical-chemical characteristics given to the membranes, was in function of the biological effect pretended in the effector tissue.
The two types of membranes, synthetized for the elaboration of the bilaminar implant, were elaborated with biomedical grade chitosan of medium molecular weight with 75-85% of deacetylation in powder presentation from the brand Sigma Aldrich®, U.S.A.
In the case of the membrane with flat-smooth structure, it was synthetized from a chitosan solution at 2%, the dissolution medium was diluted acetic acid (Sigma Aldrich®, U.S.A); In order to acquired a suitable solubilisation, the mix was set on a magnetic stirrer for 1 hour, posteriorly the solution was brought under the action of a sonicator at 28oc for 2 hours, until the air bubbles formed by the stirrer were completely eliminated.
For the membrane with the tridimensional-porous structure, it was synthetized from a chitosan solution at 4%, the dissolution medium was diluted acetic acid (Sigma Aldrich®, U.S.A); for a suitable solubilisation, the mix was set on a magnetic stirrer for 4 hours, afterward the solution was brought under the action of a sonicator at 28oc for 2 hours, until the air bubbles formed by the stirrer were completely eliminated.
Once the solutions were elaborated, for the synthesis of the two membranes (the flat-smooth and the tridimensional-porous) both were set in a constant quantity of ml/cm2 in a Petri dish, in the case of the flat-smooth membrane, it was brought under a procedure of drying with 98% of humidity loss and for the tridimensional-porous, a procedure of phase separating was termical induced.
When both membranes are already elaborated, it is proceed to synthetize the bilaminar implant, the membranes are combined using a solution of chitosan acetate at 2%, that was distributed uniformly between both membranes to create a sandwich structure, consecutively the ensemble was put in a Petri dish and the cover was set inverted in the superior aspect of petri dish. It was set for drying for 24 hours at room temperature and then it was precipitated in a solution of sodium hydroxide 1N, following the same indications used for each membrane separately.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Csf Leakage
Keywords
chitosan, endoscopic, sellar tumor, biomaterials, transphenoidal
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Use of a novel bilaminar chitosan scaffold in the repair of the sellar floor after an endoscopic endonasal transsphenoidal surgery for a suspected hipofisary macroadenoma.
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Patient with bilaminar chitosan implant
Arm Type
Experimental
Arm Description
A 65 year old woman, right handed, started with progressive bilateral visual loss in her temporal field, over 10 months, she underwent an MRI and it was found a sellar lesion that compressed the optic chiasm, an endoscopic endonasal transsphenoidal surgery was done for the resection of the lesion, using a novel bilaminar chitosan scaffold to assist the closure of the sellar floor.
Intervention Type
Other
Intervention Name(s)
Implant of bilaminar chitosan scaffold
Other Intervention Name(s)
Endoscopic endonasal transphenoidal surgery
Intervention Description
The patient underwent endoscopic endonasal transsphenoidal surgery for resection of the sellar lesion, under the direct visualization, the lesion appeared redish and soft with moderately bleeding, a sample was taken for pathology and the remaining is extracted without complications, then the scaffold is implanted in the site of the bone defect in the sphenoid sinus, due to its moldable nature, it was easily set, covering the entire extension of the defect, a fat graft was set in the sphenoid sinus covering the bilaminar chitosan membrane, then fibrin sealant was used for hemostatic control and a nasal packing was set in both nostrils for finalize the procedure.
Primary Outcome Measure Information:
Title
Brain MRI with and without contrast
Description
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the preoperative tumor size
Time Frame
1 day preoperative
Title
Brain MRI with and without contrast
Description
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor size
Time Frame
1 day postoperative
Title
Head CT scan
Description
Bone window was used to see the repair of bone defect after surgery
Time Frame
1 month postoperative
Title
Brain MRI with and without contrast
Description
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Time Frame
1 month postoperative
Title
Brain MRI with and without contrast
Description
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Time Frame
6 months postoperative
Title
Brain MRI with and without contrast
Description
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Time Frame
1 year postoperative
Title
Brain MRI with and without contrast
Description
Axial-coronal-sagittal MRI in T1,T2 signals-measure of the postoperative tumor
Time Frame
2 years postoperative
Title
Head CT scan
Description
Bone window was used to see the repair of bone defect after surgery
Time Frame
6months postoperative
Title
Head CT scan
Description
Bone window was used to see the repair of bone defect after surgery
Time Frame
1 year postoperative
Title
Head CT scan
Description
Bone window was used to see the repair of bone defect after surgery
Time Frame
2 years postoperative
Secondary Outcome Measure Information:
Title
Visual field test
Description
visual field testing looking for compression of optic chiasm
Time Frame
1 day preoperative, follow up: 1 day postoperative, 15 days postoperative, 1 month postoperative, 6 months postoperative, 1 year postoperative, 2 years postoperative.
Title
Snellen test
Description
visual acuity testing
Time Frame
1 day preoperative, follow up: 1 day postoperative, 15 days postoperative, 1 month postoperative, 6 months postoperative, 1 year postoperative, 2 years postoperative.
Title
Glasgow scale
Description
level of consciousness
Time Frame
1 day preoperative, follow up :1 day postoperative, 15 days postoperative, 1 month postoperative, 6 months postoperative, 1 year postoperative, 2 years postoperative.
Title
Endocrinological panel
Description
evaluation of hipofisary function
Time Frame
1 day preoperative, follow up : 1 day postoperative, 15 days postoperative, 6 months postoperative,1 year postoperative, 2 years postoperative
Title
Blood cell count
Description
For evaluation of any inflammatory reaction or infection before or after the procedure
Time Frame
1 day preoperative, follow up: 1 day postoperative , 1 month postoperative, 6 months postoperative,1 year postoperative, 2 years postoperative
Title
acute phase reactans
Description
For evaluation of any inflammatory reaction or infection before or after the procedure
Time Frame
1 day preoperative, follow up: 1 day postoperative , 1 month postoperative, 6 months postoperative,1 year postoperative, 2 years postoperative
Title
blood electrolytesand
Description
evaluation of renal function and as requirement for surgery
Time Frame
1 day preoperative, follow up: 1 day postoperative , 1 month postoperative, 6 months postoperative,1 year postoperative, 2 years postoperative
Title
liver function test
Description
evaluation of liver function and as requirement for surgery
Time Frame
1 day preoperative, follow up: 1 day postoperative , 1 month postoperative, 6 months postoperative,1 year postoperative, 2 years postoperative
Title
coagulation test
Description
secondary evaluation of liver function, inflammatory reaction or infection before and after the procedure and as requirement for surgery.
Time Frame
1 day preoperative, follow up: 1 day postoperative , 1 month postoperative, 6 months postoperative,1 year postoperative, 2 years postoperative
Title
seric creatinine
Description
evaluation of renal function and as requirement for surgery
Time Frame
1 day preoperative, follow up: 1 day postoperative , 1 month postoperative, 6 months postoperative,1 year postoperative, 2 years postoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
male/female patient candidate for an endoscopic endonasal transphenoidal surgery, who need repair of the sellar floor as part of the surgical procedure.
Exclusion Criteria:
Diabetes, heart diseases, immunological diseases, infectious diseases, bone diseases.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodrigo Ramos Zuñiga, M.D. PhD
Organizational Affiliation
University of Guadalajara
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Brenda Vega Ruiz, PhD
Organizational Affiliation
University of Guadalajara
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ivan Segura Duran, M.D.
Organizational Affiliation
University of Guadalajara
Official's Role
Principal Investigator
Facility Information:
Facility Name
Departamento de neurociencias
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44340
Country
Mexico
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
complete MRI sequences, laboratory studies, visual field tests, complete biomaterial patent registration , clinical reports.
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Links:
URL
http://www.cucs.udg.mx/instituto-de-neurociencias-traslacionales
Description
website of our institute of traslational neurosciences
URL
http://www.cucs.udg.mx/general/departamento-de-neurociencias
Description
website of our center
URL
http://www.hcg.udg.mx
Description
website of our hospital facilities
Learn more about this trial
Chitosan Scaffold for Sellar Floor Repair in Endoscopic Endonasal Transsphenoidal Surgery
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