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.
ID
Bron
Aandoening
sexual function in patients with vulvar lesions
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Quality of life and sexual function
Doel van het onderzoek
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.
Onderzoeksopzet
QoL questionaires before surgery, 4 months after surgery and 6 months after surgery. consult with sexologist before and after surgery.
Onderzoeksproduct en/of interventie
Quality of live questionaires and two consults with sexologist for half the group.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
--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
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
− 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
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL6370 |
| NTR-old | NTR6555 |
| Ander register | : P17ISF |