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NCT06016452RecruitingPhase 2

A Study of Chlorophyllin for the Management of Brain Radio-necrosis in Patients With Diffuse Glioma

A Prospective Phase 2 Study of Chlorophyllin for the Management of Brain Radionecrosis in Patients With Diffuse Glioma

Source: ClinicalTrials.gov · Last updated 11 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Diffuse gliomas are common tumors involving the brain. They are usually treated by surgery followed by radiation and chemotherapy. Radiotherapy is used for the treatment of brain tumors which causes damage to the tumor cells. However, radiotherapy can also affect the surrounding healthy cells in the brain, causing inflammation and swelling in the region, which is known as radio necrosis (RN). This is considered a late side effect of radiation and is seen in 10-25% of patients treated with radiation for brain tumors. Sometimes, radionecrosis can be detected on routine imaging during follow-up without new symptoms (asymptomaticRN). At the same time, in some patients, it can give rise to new symptoms like headaches, weakness, seizures,etc (symptomatic RN). The standard treatment of RN includes steroid medicines called dexamethasone, which is helpful in a proportion of patients. This is a prospective phase 2 study. This study is being conducted to investigate the ability of the drug Chlorophyllin in the treatment of radionecrosis. Chlorophyllin is a water-soluble compound obtained from the green plant pigment called chlorophyll. It has been shown to have anti-cancer, anti-bacterial, anti-viral, anti-inflammatory, and antioxidant properties. It is also used as an oral formulation and is an over-the-counter drug in various countries, and also as a food colouring agent. This is the first time chlorophyllin will be used in the setting of brain radionecrosis. Our primary aim of the study is to assess whether CHL will improve the clinical-radiological response rates. This study will be conducted on a population of 118 patients for a duration of 3 months. The total study duration is 2 years. The study is funded by Bhabha Atomic Research Centre (BARC).

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
118 (estimated)
First submitted
10 Aug 2023
Start date
13 Nov 2023
Primary completion date
30 Nov 2025
Lead sponsor
Tata Memorial Centre
Diseases
Glioblastoma
NCT number
NCT06016452

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 118
  • From 13 Nov 2023 to the primary completion date, 30 Nov 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindications to corticosteroids.
  • Prior treatment with bevacizumab (either for disease progression or radionecrosis)

Other illness

  • Disease progression
  • Indeterminate for radionecrosis vs disease progression

Other

  • No tissue diagnosis.
  • KPS\< 50.
  • Altered mental status with deficits in understanding or inability to consent to the study.
  • Brainstem glioma

Who the study is looking for

  • Histological diagnosis of diffuse glioma.
  • Radionecrosis on imaging with new neurological symptoms/ worsening of prior deficits (Stratum A) or
  • without new symptoms (Stratum B).
  • Karnofsky Performance Scale (KPS) ≥ 50.

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tata Memorial Hospital
Coordinator of this site? Confirm its status
MumbaiIndiaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.