No registrations found.
ID
Source
Health condition
sexual function in patients with vulvar lesions
Sponsors and support
Intervention
Outcome measures
Primary outcome
Quality of life and sexual function
Secondary outcome
not applicable
Study objective
The aim of this study is to evaluate whether consulting a sexologist will have better outcomes considering quality of life and sexual function in women who underwent surgical treatment for (pre)malignant vulvar lesions.
Study design
QoL questionaires before surgery, 4 months after surgery and 6 months after surgery. consult with sexologist before and after surgery.
Intervention
Quality of live questionaires and two consults with sexologist for half the group.
Inclusion criteria
--Age 18 years or older
− Women with HSIL, dVIN or carcinoma of the vulva
− Women who are sexually active prior to the onset of the disease and desire to be sexual active after surgery
− Women who will undergo surgery or laser vaporisation of the vulva for the first time
− Signed and written informed consent
Exclusion criteria
− Women with pre-existing sexual dysfunction
− Women with advanced disease (FIGO stage IV)
− Women who need adjuvant radiotherapy (of which we know of on forehand)
− Women with a recurrent vulvar disease
− Women who are unable to understand the Dutch language
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL6370 |
| NTR-old | NTR6555 |
| Other | : P17ISF |