uterine cervical and endometrial cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients who are performed pelvic lymh node dissection, with stage 1-2 squamous cell carcinoma or adenocarcinoma of uterine cervix. 2) Patients who are performed pelvic (with or without para aoritc) lymph node dissection, with endometrial carcinoma of uterine body. 3) Patoemts aged frp, 20 to 70, with Performance status 0, give consent in writing.(1 and/or 2) +3
Exclusion criteria
Exclusion criteria: 1) Patients with a primary lymphedema or a past history of lymphedema due to infection. 2) Patients who are regarded as inadequate due to other reasons (e.g. severe varix of llower extremities).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of thes study is to compare the cumulative incidences of lymphedema between the open peritoneum method (including use of hyaluronic acid-carboxycellulose membrane) and the closed peritoneum method during anthree-year postoerative period. The lymphedema is diagnosed by medical doctors according to the criteria of this study. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoint of this stydy is as follows, evaluation of the degree of lymphedema, investigation of the relationship between the incidences of lymphocyst and lymphedema of lower extremities,investigation of the relationship between the incidences of Trichophyton infection on the foot and lympyedema of lower extremities. | — |
Countries
Japan
Contacts
The Tokyo Jikei University School of Medicine Kashiwa Hospital, Dept. of OB. & GYN.