PS 0-1 uterine cervical cancer, vaginal reconstruction, laparoscopic surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who strongly desire to maintain sexual function after surgery 2. Histopathological diagnosis of cervical cancer has been obtained. 3. FIGO classification (FIGO2008), advanced stage IA, IB1, IIA1 stage 4. Tumor diameter is 2 cm or less in preoperative evaluation 5. No marked cervical stromal infiltration of the tumor was observed in the preoperative evaluation 6. Preoperative diagnostic imaging shows no lymph node metastasis or distant metastasis 7. ECOG PS 0-1 at the time of consent acquisition 8. The age at the time of obtaining consent is 20 years old or older and 70 years old or younger. 9. The consent of the person has been obtained for participation in this research.
Exclusion criteria
Exclusion criteria: 1. The principal investigator or the investigator has determined that participation in this research is inappropriate. 2. Informed consent can't be obtained. 3. It is judged that there is an extremely high possibility of performing postoperative adjuvant therapy after surgery. 4. Have a mental illness that affects will confirmation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anatomical vaginal length immediately after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| Vaginal shortening rate and anatomical vaginal length 1 year after surgery Presence / absence / frequency of sexual life Presence or absence of sexual dysfunction 1 year after surgery Incidence of adverse events during surgery Incidence of adverse events during follow-up 1 year after surgery Tumor recurrence rate Presence or absence of postoperative adjuvant therapy | — |
Contacts
Federation of National Public Service Personnel Mutual Aid Associations, Tachikawa Hospital