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NCT05986318RecruitingPhase 2

Reducing Respiratory Symptoms of Pulmonary Irradiation in Interstitial Lung Disease

Reducing Respiratory Symptoms of Pulmonary Irradiation in Interstitial Lung Disease: A 2x2 Factorial Randomized Phase II Trial Testing N-Acetyl Cysteine and Dexamethasone

Source: ClinicalTrials.gov · Last updated 26 Aug 2026

Brief summary (registry, in English)

In this double-blind phase II randomized controlled trial, patients with lung cancer or ≤2 oligometastatic pulmonary lesions and a concomitant diagnosis of ILD who are planned for radical Radiation Therapy (RT) will be randomized using a 2 x 2 factorial design to oral N-acetylcysteine (NAC) versus placebo, and also to short course corticosteroids versus placebo.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
98 (estimated)
First submitted
1 Aug 2023
Start date
7 Jan 2025
Primary completion date
1 Jul 2028
Lead sponsor
David Palma
Diseases
Lung cancer
NCT number
NCT05986318

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 98
  • From 7 Jan 2025 to the primary completion date, 1 Jul 2028
  • 4 sites 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

  • Prior lung radiotherapy
  • Current use of oral or intravenous corticosteroids
  • Pregnancy
    • If not pregnant, use of effective contraception methods for women of childbearing age is required which can include:
    • hormonal methods (e.g. oral, injected, implanted),
    • placement of an intrauterine device,
    • barrier methods (i.e. condoms),
    • sterilization of the partner (e.g. previous vasectomy)
    • abstinence
    • Women who become pregnant should stop taking NAC and/or dexamethasone and inform their study doctor.
    • Male participants should use adequate forms of birth control with their partners.
  • Contraindications to dexamethasone or N-Acetyl Cysteine (NAC). These include:
    • Previous intolerance or allergy to dexamethasone or NAC
    • Scleroderma
    • Active infection
    • Glaucoma
    • Psychiatric disorder that could be exacerbated by dexamethasone
    • Cystinuria
    • Any other condition that the treating physician believes to be a contraindication to dexamethasone or NAC

Other illness

  • Plans for the patient to receive other local therapy to the target lesion(s) while on this study, except at disease progression
  • Any medical condition that could, in the opinion of the investigator, preclude radiotherapy or prevent follow-up after radiotherapy

Other

  • Currently breastfeeding
  • Current or recent use of NAC

Who the study is looking for

  • Lung cancer or 1-2 oligometastatic pulmonary lesions planned for radical intent radiotherapy \[minimal Biologically Effective Does (BED) of 48 Gy10 (Gray) or biological equivalent\].
  • Pathologically (histologically or cytologically) proven diagnosis of cancer is not required, but strongly recommended.
    • If the risk of biopsy is unacceptable, pathologic confirmation is not required providing there is growth over time on Computed Tomography (CT) imaging and/or Fluorodeoxyglucose (FDG) avidity that is strongly suggestive of malignancy.
  • Fibrotic Interstitial Lung Disease (ILD) of any subtype, as diagnosed by a respirologist and confirmed by central review
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-3
  • Age ≥ 18
  • Life expectancy \> 6 months
  • Patients are allowed to receive anti-fibrotic agents used in the treatment of Idiopathic Pulmonary Fibrosis (IPF) or non-IPF fibrotic ILD (e.g. nintedanib, pirfenidone) and/or corticosteroids, if those are part of their current ILD treatment regimen. Other immunosuppressive drugs such as mycophenolate, azathioprine, cyclophosphamide, and rituximab must be stopped for 2 weeks prior and 2 weeks after Radiation Therapy (RT).
  • Concurrent standard chemotherapy is allowed where indicated. All other systemic therapies, including biologic targeted agents or immunotherapy, or any drugs with known radiosensitive effects, must be stopped for 2 weeks prior and 2 weeks after treatment.

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

Full criteria on ClinicalTrials.gov

Sites (4)

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

SiteCityCountrySite status
Verspeeten Family Cancer Centre, London Health Sciences Centre
Coordinator of this site? Confirm its status
LondonCanadaRecruiting
Centre Hospitalier de l'Universite de Montreal (CHUM)
Coordinator of this site? Confirm its status
MontrealCanadaRecruiting
Saint John Regional Hospital-Horizon Health Network
Coordinator of this site? Confirm its status
Saint JohnCanadaRecruiting
BC-Cancer Agency - Vancouver
Coordinator of this site? Confirm its status
VancouverCanadaRecruiting

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