Clinical Feasibility of the ARCHITECT Applicator in Cervical Cancer Brachytherapy
Starting soon · Not applicable
Conditions studied: Locally Advanced Cervical Cancer, Uterine Carcinoma
In brief
This prospective, non-randomised, single centre, phase I trial assesses the clinical feasibility of the use of the patient-tailored ARCHITECT applicator in locally advanced cervical cancer brachytherapy.
Key facts
- Study ID
- NCT07435987
- Run by
- Erasmus Medical Center
- People needed
- 25
- Starts
- 2026-05-01
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-02-27
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Locally advanced cervical cancer (FIGO 2018 stage 1B3-IVA) with indication for primary radiotherapy including brachytherapy
- Written informed consent
You may not qualify if…
- Unable to give informed consent;
- Tumour extension in the lower 2/3rd of the vagina;
- Requiring a Geneva tandem with ovoids' size 13 mm in the first application for brachytherapy;
- Known nylon allergy.
Where it is running
- Erasmus Medical Center — Rotterdam, Netherlands
Full record on ClinicalTrials.gov
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