Under construction – not a live service
Sign in
Taking people in ChinaNo phase

Spectral CT Scans to Guide Radiotherapy for Cervical Cancer

Studies spectral CT imaging for planning radiotherapy in adults with cervical cancer.

Plain-language title generated from the registry record
Registry title: Spectral CT in Radiotherapy for Cervical Cancer

Key facts

Where
Beijing, ChinaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adult women with cervical cancer confirmed by pathology who are treated with chemotherapy and radiotherapy together and have spectral CT scans.

Age
18 years or older
Sex
Women only
Disease stage
Cervical cancer confirmed by pathology. No stage is given.
Earlier treatment
Patients are treated with concurrent chemoradiotherapy. All had an 18F-FDG PET/CT before treatment.

Main reasons for not taking part

  • CT without spectral scans
  • History of allergy to intravenous contrast
  • Pregnant or potentially pregnant women

Read by machine on 9 November 2026.

Where in China

  • Peking Union Medical College HospitalBeijing, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Peking Union Medical College Hospital
Trial code
NCT06433817
Record updated
30 May 2024
Original description
The purpose of this study was to explore the potential application of spectral CT for radiotherapy in cervical cancer.Read full original descriptionShow less

The Clinical Research of Spectral CT in Radiotherapy for Cervical Cancer

The purpose of this study was to explore the potential application of spectral CT for radiotherapy in cervical cancer.

Inclusion: All patients were confirmed cervical cancer by pathology; patients were treated with concurrent chemoradiotherapy; Spectral CT scans acquisition performed during the arterial phase and venous phase; All the patients underwent a 18F-FDG PET/CT before treatment.

Exclusion: History of allergy to intravenous contrast; CT without spectral scans; Pregnant or potentially pregnant female subjects.

ClinicalTrials.gov NCT06433817