# A New Patient Reported Outcome Instrument to Assess Symptom Experience in Women With Vulvar Neoplasms (WOMAN-PRO)

> **NCT01300663** · — · UNKNOWN · sponsor: **University of Basel** · enrollment: 150 (estimated)

## Conditions studied

- Women With Vulvar Intraephitelial Neoplasia or Vulvar Cancer

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT01300663
- **Lead sponsor:** University of Basel
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2009-01
- **Primary completion:** 2011-12
- **Final completion:** 2011-12
- **Target enrollment:** 150 (ESTIMATED)
- **Last updated:** 2011-02-23

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01300663

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01300663, "A New Patient Reported Outcome Instrument to Assess Symptom Experience in Women With Vulvar Neoplasms (WOMAN-PRO)". Retrieved via AI Analytics 2026-08-01 from https://api.ai-analytics.org/clinical/NCT01300663. Licensed CC0.

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