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A prospectie, randomized control, multicenter clinical study: the preventive and therapeutic effect of thalidomide to the radiation-induced oral mucous of nasopharyngeal carcinoma

A prospectie, randomized control, multicenter clinical study: the preventive and therapeutic effect of thalidomide to the radiation-induced oral mucous of nasopharyngeal carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17011696
Enrollment
Unknown
Registered
2019-06-19
Start date
2017-07-01
Completion date
Unknown
Last updated
2019-11-18

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

Conditions

radiation-induced oral mucositis

Interventions

Drug Group :thalidomide (75mg, qn) and mouthwash from Day 1 of radiation therapy to week 6-7
Control Group:mouthwash from Day 1 of radiation therapy to week 6-7

Sponsors

Sixth Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years old; 2. Patients with histologically locally advanced NPC; 3. willing to accept the treatment as this study provide; 4. KPS score of 70 or more; 5. reexamination on time; 6. fill out the scales by self or with others help; 7. Adequate hematologic function (PLT=70×109 per liter;ANC=1.5×109 per liter); 8. sign the informed consent

Exclusion criteria

Exclusion criteria: 1. Women during Pregnancy, breastfeeding or those of childbearing age who do not want to take contraceptive measures; 2. Patients with any Mental problem; 3. Patients with substance abuse or alcohol abuse; 4. Patients with some other certain oral diseases; 5. Patients recieved glucocorticoids or immunosuppressor in the last month; 6. Patients Allergic to the drug ingredients; 7. Patients had Participated in other drug clinical trials in the past 4 weeks; 8. Patients had a history of venous or arterial thrombosis.

Design outcomes

Primary

MeasureTime frame
visual analogue scale(VAS);RTOG Grade;

Secondary

MeasureTime frame
adverse reactions;quality of life;drug combination;

Countries

China

Contacts

Public ContactLeifeng, Liang

Sixth Affiliated Hospital of Guangxi Medical University

liangleifeng170@163.com+86 13657757927

Outcome results

None listed

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