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Recruiting NCT06413212

NCT06413212 Exploratory Study of Precise Therapy for Advanced Tumor Patients With Malignant Hydrothorax or Ascites by Using PTC Drug Sensitivity Testing

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Clinical Trial Summary
NCT ID NCT06413212
Status Recruiting
Phase
Sponsor Liu Huang
Condition Lung Cancer
Study Type OBSERVATIONAL
Enrollment 55 participants
Start Date 2023-08-04
Primary Completion 2025-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Patient-derived tumor-like cell clusters (PTC) drug sensitivity testing.

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 55 participants in total. It began in 2023-08-04 with a primary completion date of 2025-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

To explore the consistency between result of PTC drug screening tests and actual clinical outcome for patients with advanced malignancy.

Eligibility Criteria

Inclusion Criteria: 1. 18 to 75 years old, regardless of gender. 2. Score of nutrition risk screening 2002 (NRS2002) is less than 3, NRS20023. 3. Advanced and unresectable malignancy confirmed by biopsy diagnosis. 4. Able to tolerate anti-tumor treatment, and without serious cardiopulmonary and other underlying diseases. 5. Score of eastern cooperative oncology group (ECOG) is not higher than 2, ECOG≤2. 6. Anticipated survival exceed six months. 7. At least one measurable lesions (according to RECIST 1.1) 8. Resistance or intolerance to standard therapy regimens. 9. Signed informed consent form voluntarily. Exclusion Criteria: 1. Pregnant or lactating women. 2. Have Participated other clinical trials in six months. 3. Severe liver dysfunction. 4. Severe renal dysfunction. 5. Patients with cognitive disorder, mental diseases and terrible compliance. 6. Allergic to known chemotherapeutic agents. 7. Other circumstance not suitable to participate in this trial determined by investigators.

Contact & Investigator

Central Contact

Liu Huang

✉ huangliu@tjh.tjmu.edu.cn

📞 63639656

Principal Investigator

Liu Huang

PRINCIPAL INVESTIGATOR

Tongji Hospital

Frequently Asked Questions

Who can join the NCT06413212 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Lung Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06413212 currently recruiting?

Yes, NCT06413212 is actively recruiting participants. Contact the research team at huangliu@tjh.tjmu.edu.cn for enrollment information.

Where is the NCT06413212 trial being conducted?

This trial is being conducted at Wuhan, China.

Who is sponsoring the NCT06413212 clinical trial?

NCT06413212 is sponsored by Liu Huang. The principal investigator is Liu Huang at Tongji Hospital. The trial plans to enroll 55 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology