Clinical trial · Interventional
Minimally Invasive Radical Hysterectomy Using Endoscopic Stapler in Stage IB2 or IIA1 Cervical Cancer
A Multicenter Non-inferiority Randomized Controlled Trial on Minimally Invasive Radical Hysterectomy Using an Endoscopic Stapler to Prevent Tumor Spillage in Stage IB2-IIA1 Cervical Cancer
- 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)
This study is a multicenter, open-label, non-inferiority, randomized controlled, investigator-initiated clinical trial comparing the efficacy and safety of open radical hysterectomy versus minimally invasive radical hysterectomy using an endoscopic stapler as surgical treatments for early cervical cancer.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer Stage IB2 | Malignant Cervical Neoplasm | CURATED_BROADER | 0.78 |
| Cervical Cancer Stage IIa | Malignant Cervical Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Minimally invasive radical hysterectomy | Device | — | UNRESOLVED |
| Open radical hysterectomy | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Open radical hysterectomy
- description
- Radical hysterectomy is performed via open surgery
- interventionNames
- Device: Open radical hysterectomy
- type
- EXPERIMENTAL
- label
- Minimally invasive radical hysterectomy
- description
- Radical hysterectomy is performed via minimally invasive surgery
- interventionNames
- Device: Minimally invasive radical hysterectomy
Primary outcomes (1)
- measure
- 4.5-year progression-free survival rate
- timeFrame
- Up to 4.5 years after enrollment
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 20 Years
Show eligibility criteria text
I. Inclusion Criteria: 1. 2018 FIGO stage IB2 or IIA1 cervical cancer (tumor maximum diameter ≥2 cm and \<4 cm) 2. Histologically confirmed squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma 3. Planned for Type B or C radical hysterectomy 4. With adequate bone marrow, renal, and hepatic function * WBC \>3.0 × 10⁹ cells/L * Platelets \>100 × 10⁹ cells/L * Creatinine \<180 μmol/L * Bilirubin \<1.5 × normal range * AST, ALT \< 3 × normal range 5. Eastern Cooperative Oncology Group (ECOG) performance status 0-2 6. Previous history of other invasive malignancies with no evidence of recurrence for at least 5 years 7. Signed and approved consent form II. Exclusion Criteria: 1. Histological types other than squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma 2. Tumor size less than 2 cm classified as 2018 FIGO stage IA1, IA2, or IB1 disease 3. The following are observed on preoperative CT or MRI * Tumor size ≥4 cm * Lymph node metastasis (short axis ≥15 mm) * Paracervical invasion * Bladder or rectal invasion * Distant metastasis 4. Prior pelvic or abdominal radiotherapy 5. Prior neoadjuvant chemotherapy before surgery 6. Unsuitable for surgery due to severe systemic disease at the investigator's discretion 7. Difficult to consider intraoperative lymphatic mapping due to * Allergy to triphenylmethane compounds * History of prior retroperitoneal surgery * History of prior pelvic radiotherapy * Cases where cold knife or loop electrosurgical excision procedure (LEEP) was performed within 4 weeks prior to study participation * Allergy to triphenylmethane compounds
References
Publications (0)
Data not yet available