Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:26 AM
Ignite Modification Date:
2025-12-25 @ 12:26 AM
NCT ID:
NCT05355558
Eligibility Criteria:
Inclusion Criteria:
* Have given written informed consent, with the understanding that consent may be withdrawn at any time without prejudice
* Histologically or cytologically confirmed cervical carcinoma
* FIGO staged IB to IVA
* Underwent MRI pelvis
* Underwent FDG-PET/CT or MRI abdomen or CT thorax and abdomen or Chest X ray for routine staging
* Planned for radical radiotherapy with or without chemotherapy
* No distant metastasis in staging work up
* ECOG 0-2
* Age 21 or over (no upper age limit)
Exclusion Criteria:
* Patients scheduled for neoadjuvant chemotherapy
* Patients with previous hysterectomy or radiotherapy to the pelvis
* Patients who are pregnant or lactating
* Patients who do not meet the above mentioned inclusion criteria
* Patients who refuse to give and/or sign the informed consent
* Patients who currently have a pacemaker
* Patients who have a history of serious adverse events related to a previous MRI or PET/CT
* Patients who are unable to undergo MRI scanning
* Patients with a known allergy against any component of the contrast enhancing agent
* Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow up schedule; these conditions should be discussed with the patient before registration in the trial.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
21 Years
Maximum Age:
99 Years
Study:
NCT05355558
Study Brief:
Protocol Section:
NCT05355558