NCT00604994
Who may be able to join
Who might be able to join this trial:
- You are scheduled to have surgery for a gynaecological condition (either non-cancerous or cancerous), agreed upon by you and your surgeon.
- You are female and not pregnant.
- You are 18 years of age or older at the time of your surgery.
- You understand what the study involves and are willing to attend all required follow-up appointments for the full duration of the study.
- You are able to give your own informed consent to take part in the study.
Who may not be able to join:
- You have a pacemaker fitted.
- You have a known allergy to adhesive electrode pads (the sticky patches placed on the skin) or have large metal plates inside your body, as these may interfere with a specific type of monitoring used in the study (confirm with trial site).
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Trial details
Where this trial is recruiting
6 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Time of onset of lymphoedema after gynaecological cancer treatment.; Incidence of lymphoedema after gynaecological cancer treatment.; Point prevalence of lymphoedema after gynaecological cancer treatment.; Severity of lymphoedema after gynaecological cancer treatment.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.