First Line Ovarian Cancer Treatment - Cohort Study

NCT ID: NCT01832415

Last Updated: 2016-03-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-04-30

Study Completion Date

2016-03-31

Brief Summary

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The French cooperative group GINECO proposes to implement an observational study to describe a real situation, in daily practice tolerance and methods of administration of bevacizumab (Avastin ®)

Detailed Description

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Population: Patients aged 18 years and older with an epithelial ovarian cancer, fallopian tube or primary peritoneal or witch it was decided to initiate a process comprising of Bevacizumab (Avastin ®) in first-line therapy

Conditions

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Epithelial Ovarian Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Use of bevacizumab (Avastin ®) - First-line ovarian cancer

Patient receiving bevacizumab in ovarian cancer first line treatment

Bevacizumab

Intervention Type DRUG

Observation of bevacizumab administration in first line ovarian cancer treatment

Interventions

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Bevacizumab

Observation of bevacizumab administration in first line ovarian cancer treatment

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients aged 18 years and over,
* Patients with an epithelial ovarian cancer, fallopian tube or peritoneal who will receive bevacizumab (Avastin ®) in first-line therapy
* Patients should be informed of the study orally and should not have any objection their data to be processed.

Exclusion Criteria

* Patient participation in a clinical trial
* Patient non-affiliated to a social security scheme.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Roche Pharma AG

INDUSTRY

Sponsor Role collaborator

ARCAGY/ GINECO GROUP

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dominique BERTON-RIGAUD, MD

Role: PRINCIPAL_INVESTIGATOR

ICO de l'Ouest, Site René Gauducheau - Saint-Herblain

Locations

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Centre Paul Papin

Angers, , France

Site Status

Clinique Tivoli

Bordeaux, , France

Site Status

Institut Bergonié

Bordeaux, , France

Site Status

Centre jean Perrin

Clermont-Ferrand, , France

Site Status

Centre Hospitalier Intercommunal

Fréjus, , France

Site Status

institut Paoli Calmette

Marseille, , France

Site Status

Clinique Valdegour

Nîmes, , France

Site Status

Centre Hospitalier Régional

Orléans, , France

Site Status

Arcagy-Gineco

Paris, , France

Site Status

Centre Hospitalier Lyon-sud

Pierre-Bénite, , France

Site Status

Institut Jean Godinot

Reims, , France

Site Status

Clinique Armoricaine de Radiologie

Saint-Brieuc, , France

Site Status

ICO René Gauducheau

Saint-Herblain, , France

Site Status

Hôpital Civil

Strasbourg, , France

Site Status

Countries

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France

References

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Berton D, Floquet A, Lescaut W, Baron G, Kaminsky MC, Toussaint P, Largillier R, Savoye AM, Alexandre J, Delbaldo C, Malaurie E, Barletta H, Bosacki C, Garnier-Tixidre C, Follana P, Laharie-Mineur H, Briac Levache C, Valenza B, Dechartres A, Mollon-Grange D, Selle F. Real-World Experience of Bevacizumab as First-Line Treatment for Ovarian Cancer: The GINECO ENCOURAGE Cohort of 468 French Patients. Front Pharmacol. 2021 Sep 20;12:711813. doi: 10.3389/fphar.2021.711813. eCollection 2021.

Reference Type DERIVED
PMID: 34616296 (View on PubMed)

Other Identifiers

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ENCOURAGE (GINECO-OV123)

Identifier Type: -

Identifier Source: org_study_id

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