Database of patients with cervical cancer at Institut Paoli Calmettes

Institut Paoli Calmettes Cervical Cancer Database

Observational Institut Paoli-Calmettes · NCT02869490

This study is creating a detailed database of cervical cancer patients to help understand the disease better and improve treatment for future patients.

Quick facts

Study typeObservational
Enrollment6000 (estimated)
Ages18 Years to 95 Years
SexFemale
SponsorInstitut Paoli-Calmettes Academic / other
Locations1 site (Marseille, Bouches du Rhone)
Trial IDNCT02869490 on ClinicalTrials.gov

What this trial studies

This observational study focuses on creating a comprehensive database of patients diagnosed with cervical cancer at the Institut Paoli Calmettes. The database will collect and organize clinical data to better understand the disease and improve patient outcomes. By gathering detailed information on patient demographics, treatment regimens, and outcomes, the study aims to facilitate future research and enhance clinical practices related to cervical cancer.

Who should consider this trial

Good fit: Ideal candidates for this study are patients who have been diagnosed with cervical cancer.

Not a fit: Patients who do not have a diagnosis of cervical cancer will not benefit from this study.

Why it matters

Potential benefit: If successful, this database could lead to improved understanding and treatment strategies for cervical cancer patients.

How similar studies have performed: While this approach is primarily observational and may not have direct therapeutic interventions, similar databases have been successful in enhancing understanding and treatment of various cancers.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient with a diagnosis of cervical cancer

Exclusion Criteria:

* Non applicable

Where this trial is running

Marseille, Bouches du Rhone

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Uterine Cervical Neoplasms
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.