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Recruiting NCT06950814

NCT06950814 Prognostic Impact of Adjuvant Therapy in Primary Hepatic Sarcomatoid Carcinoma

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Clinical Trial Summary
NCT ID NCT06950814
Status Recruiting
Phase
Sponsor West China Hospital
Condition Sarcomatoid Carcinoma
Study Type OBSERVATIONAL
Enrollment 50 participants
Start Date 2025-04-05
Primary Completion 2025-05-03

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
postoperative adjuvant therapy

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 50 participants in total. It began in 2025-04-05 with a primary completion date of 2025-05-03.

⚠ 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

In recent years, researchers have conducted extensive studies on adjuvant therapy following surgical resection of liver cancer, exploring its potential benefits and seeking effective treatment strategies. Given the rarity and high aggressiveness of primary hepatic sarcomatoid carcinoma, there is a lack of reliable clinical evidence on whether postoperative adjuvant therapy can benefit patients, resulting in the absence of established standard guidelines. Therefore, we conducted a single-center retrospective study to assess the potential benefits of postoperative adjuvant therapy for patients of primary hepatic sarcomatoid carcinoma.

Eligibility Criteria

Inclusion Criteria: 1. patients who underwent liver resection 2. patients' postoperative paraffin pathology and immunohistochemistry results were reviewed to identify those diagnosed with PHSC Exclusion Criteria: 1. patients who received other anti-tumor treatments before surgery, such as radiofrequency ablation (RFA), transarterial chemoembolization (TACE), radiation therapy (RT), and systemic therapy; 2. patients diagnosed with other specific types of sarcomas; 3. patients with concurrent other malignancies during the course of PHSC; 4. patients who were lost to follow-up or lacked essential clinical data.

Contact & Investigator

Central Contact

Jiwei Huang Professor

✉ huangjiwei@wchscu.cn

📞 +86 18980606725

Frequently Asked Questions

Who can join the NCT06950814 clinical trial?

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

Is NCT06950814 currently recruiting?

Yes, NCT06950814 is actively recruiting participants. Contact the research team at huangjiwei@wchscu.cn for enrollment information.

Where is the NCT06950814 trial being conducted?

This trial is being conducted at Chengdu, China.

Who is sponsoring the NCT06950814 clinical trial?

NCT06950814 is sponsored by West China Hospital. The trial plans to enroll 50 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: April 2026  ·  Data Methodology