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NCT06230549: ProART

Adaptive Radiotherapy in Patients With Gynecological Tumors

Recruiting now NA Last updated 9 February 2024
What this trial tests

NA trial testing Adaptive Radiotherapy in Gynecological Tumor in 30 participants. Currently enrolling.

Timeline
15 January 2024
Primary endpoint
15 December 2024
15 December 2026

Quick facts

Lead sponsorUniversity Hospital, Essen
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposetreatment
Enrollment30
Start date15 January 2024
Primary completion15 December 2024
Estimated completion15 December 2026
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Essen

Who can join

18 and older, female only, with Gynecological Tumor or Adaptive Radiotherapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Prospective randomized evaluation of adaptive radiotherapy in the definitive radiotherapy of locally advanced gynecologic carcinoma (e.g. cervical carcinoma, endometrial carcinoma, vaginal carcinoma), in the postoperative situation or first series of external beam radiotherapy and in patients in whom radical surgery or HDR brachytherapy as dose boost is not an option.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Adaptive Radiotherapy

Trials testing the same drug.

Other University Hospital, Essen 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/NCT06230549.

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