Neoadjuvant Therapy in Cervical Cancer
Recruiting
N/A
Interventional Study
Uterine Cervical Neoplasms
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 70
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 48 (estimated)
- Sponsor
- Qilu Hospital of Shandong University · Other
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About This Trial
In the comprehensive dataset of clinical diagnoses and treatments for cervical cancer in China, 49.8% of patients with stage IB3 and IIA2 receive surgical intervention following neoadjuvant chemotherapy. This indicates a pressing need to optimize neoadjuvant chemotherapy regimens for locally advanced cervical cancer. While paclitaxel combined with cisplatin is the conventional approach, 9.8% to 30…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Clinical diagnosis of cervical squamous cell carcinoma
* HER-2 positive
Exclusion Criteria:
* Cervical adenocarcinoma
Contacts