Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
25 participants
OBSERVATIONAL
2014-05-31
2019-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
OTHER
Study Groups
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With ALA
Patients with malignant glioma. 25 patients will be provided the ALA for inducing fluorescence
ALA
Prior to surgery all patients would receive freshly prepared solution of 5-ALA, 20 mg/kg bodyweight dissolved in 100 ml of potable water orally approximately 4 hours (range 4-6 hrs) before the commencement of anesthesia induction for surgery.
The surgery would then be performed with the help of navigation. After craniotomy, the navigation software would be used to identify the selected target areas based on the preoperative images (MR as well as PET when available) and directed image-guided biopsies from these representative areas will be collected for histological evaluation
Without ALA
5 tumor tissue samples from ACTREC tumor tissue repository will be obtained. These would be malignant gliomas or other brain tumor samples where ALA is usually not administered and will be used as controls and for calibration purposes
No interventions assigned to this group
Interventions
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ALA
Prior to surgery all patients would receive freshly prepared solution of 5-ALA, 20 mg/kg bodyweight dissolved in 100 ml of potable water orally approximately 4 hours (range 4-6 hrs) before the commencement of anesthesia induction for surgery.
The surgery would then be performed with the help of navigation. After craniotomy, the navigation software would be used to identify the selected target areas based on the preoperative images (MR as well as PET when available) and directed image-guided biopsies from these representative areas will be collected for histological evaluation
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Adults (18-65 years)
* Radiologically suspected malignant gliomas
* Variable contrast enhancement on MRI (patchy and/or non-uniform)
* Eligible for surgical therapy (craniotomy NOT stereotactic biopsy )
* No contraindication for surgery
Exclusion Criteria
* Prior treatment (except biopsy)
* Compromised renal/hepatic function
* Immunocompromised status
* Known photosensitivity / allergy to 5-ALA
18 Years
65 Years
ALL
No
Sponsors
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Tata Memorial Hospital
OTHER_GOV
Responsible Party
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Dr Aliasgar V Moiyadi
Prof Neurosurgery
Principal Investigators
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Aliasgar V Moiyadi, MCh DNB
Role: PRINCIPAL_INVESTIGATOR
neurosurgeon
Locations
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Advanced Centre for Treatment, Research & Education in Cancer (ACTREC)
Navi Mumbai, Maharashtra, India
Countries
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Other Identifiers
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TMC- ACTREC IRB project no 139
Identifier Type: -
Identifier Source: org_study_id
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