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Prospective study of clinical and pathological characteristics of salivary gland carcinoma in oral and maxillofacial region.

Prospective study of clinical and pathological characteristics of salivary gland carcinoma in oral and maxillofacial region.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017851
Enrollment
Unknown
Registered
2018-08-17
Start date
2018-10-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

salivary gland carcinoma in oral and maxillofacial region

Interventions

Case series:Nil

Sponsors

Shanghai Jiao Tong University, School of Medicine, Shanghai Ninth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Aged 20 to 80 years old male and female; (2) diagnosis of oral salivary gland carcinoma in oral and maxillofacial region by histopathology; (3) ECOG score 0 to 2 points, is expected to live longer than 6 months; (4) clinical staging in line with local advanced (III ~ IV, refer to the seventh edition UICC / AJCC staging system [22]), including unresectable tumors; (5) before the trial signed informed consent, voluntarily participate in the test; (6) good compliance; (7) blood, blood sugar and liver, kidney, lung function and other normal; (8) female pregnancy test subjects pregnancy test negative, must agree to use effective contraceptive measures to ensure that during the trial and stop treatment within 3 months after pregnancy is not pregnant.

Exclusion criteria

Exclusion criteria: (1) failure to obtain signed informed consent; (2) pregnant, lactating women; (3) vital organs dysfunction, the existence of life-threatening; (4) patients who have received radiotherapy locally; (5) local skin ulceration, open wound; (6) clear distant metastases or other malignancies; (7) known to have allergic reactions to chemotherapy drugs; (8) suffering from mental illness, can not cooperate with the treatment; (9) have febrile disease, can not control the symptoms; (10) abnormal coagulation, bleeding tendency; (11) had participated in other clinical trials in the past 30 days; (12) other investigators believe that inappropriate treatment of the situation.

Design outcomes

Primary

MeasureTime frame
RNA expression;

Countries

China

Contacts

Public ContactWan-Tao Chen

Shanghai Jiao Tong University, School of Medicine, Shanghai Ninth People's Hospital

chenwantao196323@sjtu.edu.cn+86 021-23271699-5211

Outcome results

None listed

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