Clinical trial · Interventional
99mTc-H7ND SPECT/CT Imaging in NSCLC
99mTc-H7ND SPECT/CT Imaging in Non-small Cell Lung Cancer Clinical Application Research in Efficacy Evaluation and Efficacy Prediction
NCT05999214CI-TRIAL-00069886unknownN/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)
To study the clinical application of 99mTc-H7ND SPECT/CT imaging in the efficacy evaluation and prediction of non-small cell lung cancer (NSCLC)
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| NSCLC | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 99mTc-H7ND SPECT/CT imaging performed | Diagnostic Test | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Experimental group
- description
- 99mTc-H7ND SPECT/CT imaging was performed
- interventionNames
- Diagnostic Test: 99mTc-H7ND SPECT/CT imaging performed
- type
- NO_INTERVENTION
- label
- Control group
- description
- 99mTc-H7ND SPECT/CT imaging was not performed
Primary outcomes (1)
- measure
- DCR
- timeFrame
- Repeat visits were performed 8-12 weeks and 12 weeks after the baseline assessment
- description
- Comparison of DCR in groups of NSCLC patients with stable disease assessed by RECIST1.1.
Secondary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients aged from 18 to 80 years old; 2. patients with NSCLC confirmed by needle aspiration cytology or surgical pathology, who cannot undergo radical surgery due to recurrence, metastasis or patient's own conditions; 3. Has completed 2-4 cycles of first-line therapy (including chemotherapy, immunotherapy, chemotherapy combined with immunotherapy, chemotherapy combined with targeted therapy, etc.), and has SD assessed by RECIST 1.1 during the same period; 4. Patients had at least one measurable lesion; 5. No local radiotherapy for primary or metastatic lesions within 28 days; 6. ECOG score 0-2; 7. Expected survival time ≥3 months; 8. Voluntarily participate and sign informed consent. Exclusion Criteria: 1. Women who plan to become pregnant within 6 months, or are pregnant or lactating. 2. Patients with severe brain or bone metastases; 3. Severe anemia and severe liver and kidney damage; 4. Pathological or long-term follow-up results may not be available; 5. The relevant control imaging data and clinical data were not available; 6. Severe illness is difficult to cooperate (such as acute cardiovascular and cerebrovascular events or serious cardiovascular diseases); 7. Received any surgery or invasive treatment or procedure within 4 weeks before enrollment; 8. Cannot tolerate standard second-line therapy or other first-line therapies. 9. Known allergy to 99mTc-H7ND or any of its components; He had a history of severe allergies; 10. Protocol imaging contraindications were present; 11. The investigator considered it inappropriate to participate in the study.
References
Publications (0)
Data not yet available
No reference posted for this study.