- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00311116
Vitamin E to Prevent Mucositis in Children With Cancer
Serial Controlled N-of-1 Trials of Topical Vitamin E as Prophylaxis for Chemotherapy-induced Oral Mucositis in Pediatric Patients
Studieoversikt
Detaljert beskrivelse
Oral mucositis is a common consequence of chemotherapy and is an important sequela of cancer therapy because it is painful and affects quality of life, may lead to hospitalization for hydration or pain control, and provides a portal of entry for oral microflora. In addition, oral mucositis has become a major dose-limiting toxicity and consequently, may limit delivery of anti-cancer therapy.
Despite the frequency of mucositis, there are no feasible therapies proven to be successful in preventing mucositis in children. Vitamin E is a fat-soluble essential vitamin that may protect against doxorubicin-induced oral mucositis through its anti-oxidant properties.
In this study, we will examine the efficacy of topical vitamin E as prophylaxis against chemotherapy-induced mucositis with a novel methodology appropriate for the study of rare conditions, namely combining N-of-1 trials using Bayesian meta-analysis.
The primary outcome is an objective mucositis score measured on days 7, 10, 14 and 17. Secondary outcomes included daily pain and swallowing visual analogue scale scores, and World Health Organization mucositis scores collected on days 5 to 20.
Comparisons: Objective and subjective mucositis scores will be compared in cycles associated with topical vitamin E versus cycles associated with placebo administration. We will use repeated measures analysis within a Bayesian framework in order to conduct this comparison.
Studietype
Registrering
Fase
- Fase 2
- Fase 3
Kontakter og plasseringer
Studiesteder
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Ontario
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Toronto, Ontario, Canada, M5G 1X8
- The Hospital for Sick Children
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- diagnosis of cancer and treated at the Hospital for Sick Children, Toronto, Canada
- planned chemotherapy includes at least two identical courses of doxorubicin-containing chemotherapy in which the dose of doxorubicin was at least 60 mg/m2 per course
- at least 6 years of age and less than 18 years
- lives in the Greater Toronto area
Exclusion Criteria:
- allergy to vitamin E or placebo ingredients
- child is unable to comply with topical vitamin E application
- cild is receiving head or neck irradiation
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Dobbelt
Hva måler studien?
Primære resultatmål
Resultatmål |
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Objective mucositis score at 7, 10, 14, and 17 days post initiation of chemotherapy
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Sekundære resultatmål
Resultatmål |
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Pain visual analogue scale
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Difficulty swallowing visual analogue scale
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World Health Organization mucositis grade
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Analgesia use (topical, systemic non-narcotic or narcotic
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Receipt of intravenous fluid, and total parenteral nutrition.
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Chemotherapy decrements or delays due to mucositis
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Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Brian M Feldman, MD, MSc, The Hospital for Sick Children
Studierekorddatoer
Studer hoveddatoer
Studiestart
Studiet fullført
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 0020010130
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