Improving sexual function in patients with vulvar lesions

Improving sexual function and well-being in patients with (pre) invasive vulvar lesions; a controlled pilot study.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON26388

Enrollment

Registered

2017-07-03

Start date

2017-07-31

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sexual function in patients with vulvar lesions

Interventions

Quality of live questionaires and two consults with sexologist for half the group.

Eligibility

Inclusion criteria

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

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 outcomes

Primary

Measure	Time frame
Quality of life and sexual function	—

Contacts

Public ContactJesse van Altena

j.v.altena@nki.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)