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Study on the sensitivity and prognosis of functional MRI in chemoradiotherapy of advanced sinonasal squamous cell carcinoma

Study on the sensitivity and prognosis of functional MRI in chemoradiotherapy of advanced sinonasal squamous cell carcinoma

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033508
Enrollment
Unknown
Registered
2020-06-03
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sinonasal squamous cell carcinoma

Interventions

Recurrence group vs non recurrence group:N/A

Sponsors

Eye, Ear, Nose & Throat Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate and sign an informed consent in writing. 2. Aged 18-70 years. Gender is not limited. 3. Primary sinonasal squamous cell carcinoma confirmed by pathology or cytology. 4. The clinical-stage was IVA-IVB. 5. There are tumor volumes that can be objectively measured or evaluated. 6. Karnofsky scores >= 70. 7. The estimated survival time is more than six months. 8. The blood routine, liver, renal function, and heart function are regular: WBC > 4.0 * 10^9/L, PLT >= 100 * 10^9/L, Hgb >= 100g/L; liver function: ALT, AST 1.5 times the upper limit of standard level, total bilirubin <= 1.5 times the upper limit of standard level; renal function: serum creatinine <= 1.5 times the upper limit of the standard level. 9. Childbearing age patients should take adequate contraceptive measures. 10. Those with proper compliance are expected.

Exclusion criteria

Exclusion criteria: 1. Malignant tumor with other parts. 2. With distant metastasis. 3. With a history of mental illness. 4. Bad habits or drug use. 5. Within one month before the test, patients who have participated in other clinical trials. 6. There was previous history of allergy to biological agents or other severe history of allergy, or allergic constitution. 7. Pregnant and lactating patients, those in the childbearing period who did not take adequate contraceptive measures, and 8. Researchers think that they should not participate in this trial.

Design outcomes

Primary

MeasureTime frame
Clinical efficacy (CR, PR, SD, PD);

Secondary

MeasureTime frame
Survival evaluation (OS, PFS, DFS);

Countries

China

Contacts

Public ContactXinmao Song

Eye, Ear, Nose & Throat Hospital of Fudan University

muqinger@sina.com+86 18917785084

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026