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NCT02937948: ARCOL

Adaptative Radiotherapy for Locally Advanced Cervical Cancer

Completed NA Last updated 2 September 2022
What this trial tests

NA trial testing Adaptative treatment plan in Uterine Cervical Cancer in 85 participants. Completed in 11 April 2022.

Timeline
5 April 2017
Primary endpoint
27 May 2020
11 April 2022

Quick facts

Lead sponsorCenter Eugene Marquis
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment85
Start date5 April 2017
Primary completion27 May 2020
Estimated completion11 April 2022
Sites12 locations across France

Drugs / interventions tested

Conditions studied

Sponsor

Center Eugene Marquis — full company profile →

Who can join

18 and older, female only, with Uterine Cervical Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study evaluates the effect of adaptative Intensity-Modulated Radiation Therapy (IMRT) in the treatment of locally advanced cervical cancer on acute genito-urinary (GU), and gastrointestinal (GI) toxicities. Every patients will be treated according to the adaptative IMRT strategy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Uterine Cervical Cancer

Currently open trials in the same condition.

Other Center Eugene Marquis trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02937948.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing