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Recruiting NCT02869490

Institut Paoli Calmettes Cervical Cancer Database

Observational Uterine Cervical Neoplasms

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Data collection.
Who it may be relevant to
Registry conditions: Uterine Cervical Neoplasms. Basic parameters: 18 years — 95 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Database of Institut Paoli-Calmettes patients diagnosed with cervical cancer

Interventions

  • Other Data collection

Primary outcome measures

  • Survival of patients with cervical cancer [Time frame: 10 years]
Secondary outcome measures (1)
  • Collection of patients characteristics [Time frame: 10 years]

Eligibility criteria

Inclusion criteria

  • Patient with a diagnosis of cervical cancer

Exclusion criteria

  • Non applicable

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Institut Paoli Calmettes — Marseille

Identifiers

NCT: NCT02869490 · BDD-COL-IPC

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗