Actively Recruiting
Lymphadenectomy in Early Ovarian Cancer
Led by Sun Yat-sen University · Updated on 2021-01-15
656
Participants Needed
1
Research Sites
413 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To assess the impact of comprehensive staging surgery with no lymphadenectomy on survival and quality of life in patients with early-stage ovarian cancer.
CONDITIONS
Official Title
Lymphadenectomy in Early Ovarian Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 18 to 70 years
- Primary diagnosis of epithelial ovarian cancer FIGO stage IA to IIA
- No prior treatment or incomplete initial surgery
- Indications for adjuvant chemotherapy including high-grade serous carcinoma, grade 3 endometrioid carcinoma, clear cell carcinoma, grade 2 endometrioid carcinoma with capsule rupture or pelvic tissue extension, low-grade serous carcinoma, grade 1 endometrioid carcinoma, and mucinous carcinoma with pelvic tissue extension
- Signed and written informed consent given
- Good performance status (ECOG 0 or 1)
You will not qualify if you...
- Non-epithelial ovarian malignancies and borderline tumors
- Suspicious lymph nodes seen on preoperative imaging
- Clinically suspicious or bulky lymph nodes during surgery
- Secondary invasive cancers within the last 5 years except certain early-stage cancers
- Prior chemotherapy for ovarian cancer or pelvic/abdominal radiotherapy
- Diseases of the lymph system including unexplained lymphedema
- Prior retroperitoneal lymph node dissection
- Other medical conditions that contraindicate surgery
- Pregnancy
- Any factors preventing informed consent, protocol compliance, or regular follow-up
AI-Screening
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Trial Site Locations
Total: 1 location
1
Department of Gynecologic Oncology, Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China, 510060
Actively Recruiting
Research Team
J
Jihong Liu, Ph.D.
CONTACT
T
Ting Deng, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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