Clinical trial · Interventional
3DV+TPS Applied to Radiotherapy for Nasopharyngeal Carcinoma
3DV+TPS Applied to Radiotherapy for Nasopharyngeal Carcinoma - a Randomized, Single-blind, Multi-center Clinical Study
NCT03791944CI-TRIAL-00074279completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Verify that 3DV+TPS is non-inferior compared to existing imported TPS and superior to existing domestic TPS.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Nasopharynx Cancer | Nasopharyngeal Carcinoma | ALIAS | 0.90 |
| Radiotherapy | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 3DV + TPS / Domestic Accelerator | Device | — | UNRESOLVED |
| 3DV+TPS/VARIAN | Device | — | UNRESOLVED |
| TPS / Domestic Accelerator | Device | — | UNRESOLVED |
| TPS / VARIAN | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- 3DV+TPS/VARIAN
- description
- Use 3DV+TPS to map targets and develop treatment plans. The intervention is 3DV+TPS and VARIAN.
- interventionNames
- Device: 3DV+TPS/VARIAN
- type
- ACTIVE_COMPARATOR
- label
- TPS/VARIAN
- description
- Use imported Varian TPS to map targets and develop treatment plans.
- interventionNames
- Device: TPS / VARIAN
- type
- EXPERIMENTAL
- label
- 3DV+TPS/ Domestic accelerator
- description
- Use 3DV+TPS to map targets and develop treatment plans.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Consolidate other serious diseases that affect quality of life or treatment; 2. Reluctant to actively cooperate with the investigator; 3. Mergers with distant transfers; 4. Patients who have undergone head and neck surgery and radiotherapy; 5. Subjects who are affected by the disease who sign a written informed consent or follow the study procedure; or who are unwilling or unable to comply with the research requirements. 6. Those who have a history of psychotropic substance abuse who are unable to quit or have a mental disorder; 7. Participated in other clinical trials of anti-tumor drugs within 4 weeks before enrollment; 8. Pregnant or lactating women; 9. The investigator judges other conditions that may affect the clinical study and the outcome of the study. Exclusion Criteria: 1. Those who did not follow the protocol. 2. The subject is aggravated or has a serious adverse reaction. 3. The subject himself requested to withdraw from the trial. 4. The patient is lost to follow-up or died. 5. The researcher believes that there is reason to withdraw
References
Publications (0)
Data not yet available
No reference posted for this study.