Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT05849129

Adjunctive Intravenous Ascorbic Acid for Advanced Non-Small Cell Lung Cancer

Led by The Canadian College of Naturopathic Medicine · Updated on 2026-01-23

90

Participants Needed

1

Research Sites

365 weeks

Total Duration

On this page

Sponsors

T

The Canadian College of Naturopathic Medicine

Lead Sponsor

O

Ottawa Hospital Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a two arm RCT evaluating the effect of intravenous vitamin C versus placebo in patients with incurable non-small cell lung cancer. Participants in both arms will be receiving platinum doublet chemotherapy with or without concurrent immunotherapy as standard care. We plan to enroll 90 patients over 5 years.

CONDITIONS

Official Title

Adjunctive Intravenous Ascorbic Acid for Advanced Non-Small Cell Lung Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (≥18 years of age) with stage IIIB or IV primary non-small cell lung cancer
  • Eligible and scheduled for first line platinum-doublet chemotherapy with or without concurrent immunotherapy
Not Eligible

You will not qualify if you...

  • ECOG status greater than 2
  • Received intravenous vitamin C within 6 months prior to randomization
  • Biochemical deficiency in G6PD
  • Estimated Glomerular Filtration Rate (eGFR) less than 45 mL/min
  • Currently taking insulin or warfarin
  • History of severe renal dysfunction or hemochromatosis
  • Received cytotoxic chemotherapy or immunotherapy within 12 months prior to randomization
  • Pregnant or planning pregnancy without being a carrier of the gene for G6PD deficiency
  • Currently taking an investigational product or participating in an investigational study within the past 30 days
  • Any condition that would prevent participation as judged by the Principal Investigator or delegate

AI-Screening

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Trial Site Locations

Total: 1 location

1

The Ottawa Hospital

Ottawa, Ontario, Canada, K1H8L6

Actively Recruiting

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Research Team

D

Dugald Seely, ND, MSc

CONTACT

M

Mark Legacy, BSc, CCRP

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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