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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03250520
Other study ID # HIM 2017-072
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date September 1, 2017
Est. completion date June 28, 2022

Study information

Verified date February 2023
Source Hospital Infantil de Mexico Federico Gomez
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This Protocol is a pilot, clinical interventional study to selected patients between five and fourteen years of both sexes, carriers of the diagnosis of glioma brain stem and high grade recurrent in the central nervous system tumors, in whom there has been no response to conventional-based surgery/radiation/chemotherapy treatment or whose location does not allow treatment with conventional measures, and that already have an indication for a neurosurgical palliative procedure. It will be a close pharmacovigilance on possible adverse effects related to the nanomaterial based on the profile of cisplatin (chemotherapeutic platinum derivative), since documented toxicity data are not counted for NPt-Ca. Quality of life will be documented with PedsQL Cancer Module© and tumor size by magnetic resonance brain images.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date June 28, 2022
Est. primary completion date January 28, 2022
Accepts healthy volunteers No
Gender All
Age group 5 Years to 14 Years
Eligibility Inclusion Criteria: - Histopathological diagnosis or MRI of the brain stem or tumor of recurrent high-grade glioma. - Indication of palliative surgical treatment by neurosurgery. - Good general condition, enabling the realization of surgical treatment. - Scale Lansky > 20) - conventional treatment (surgery, radiotherapy, and chemotherapy) failed or not applicable to the patient. Exclusion Criteria: - Patients with emerging infectious diseases or fever in the last 72 hours prior to placement of the NPt-Ca. - Patients whose parents/carers do not authorize expressly the realization of procedure with knowledge of its experimental nature, are not agreed or established their commitment to meet follow-up parameters established by this Protocol. - Patients with surgical complications prior to placement of the NPt-Ca. - Patients in which the size and location of the lesion do not allow their surgical approach or an increase in volume by infiltration of the lesion with 3 ml of volume of NPt-Ca. - Patient whose neurological condition do not allow the implementation of MRI without anesthesia.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Platinum acetylacetonate (1% wt) supported by sol-gel technology functionalized titania
Sol-gel process Pt(acac)2- F-TiO2 nanostructured material with antitumoral activity used as an alternative in the treatment of cancer tumors. The biocatalysts were prepared by the sol-gel route using the complex Pt(acac)2.

Locations

Country Name City State
Mexico Hospital Infantil de Mexico Federico Gomez DF

Sponsors (1)

Lead Sponsor Collaborator
Hospital Infantil de Mexico Federico Gomez

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in the quality of life using the PedsQL Cancer Module© Measures of the change of quality of life pre and after the administration of NPt-Ca using the questionnaire PedsQL Cancer ModuleĀ© Preoperative and at 1.3, 6, 12, 18 and 24 months.
Primary Change in tumor size Change in tumor size after the administration of NPt-Ca using volumetric measures on the brain magnetic resonance. Immediate, 1, 2, 3, 6, 8, 10, 12, 18 and 24 months.
See also
  Status Clinical Trial Phase
Recruiting NCT04670016 - HRQL and Symptom Assessment for Patients With DIPG or Recurrent and Re-irradiated Brain Tumours and Their Caregivers