findmyKOL
Clinical trialNCT05197881RecruitingInterventional

Daily Adaptive Radiation Therapy an Individualized Approach for Carcinoma of the Cervix

SponsorVarian, a Siemens Healthineers CompanyEnrollment125Cervical Cancer by FIGO Stage 2018
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This is a single-arm, prospective, multi-center clinical trial designed to demonstrate that adaptive radiotherapy for locally advanced cervical cancer will translate into a decreased rate of acute gastrointestinal toxicity compared with the historically reported rate for non-adaptive intensity modulated radiation therapy (IMRT). The timepoint for this assessment will be at week 5 of external beam radiotherapy (EBRT) and will use the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

5 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of Alabama Birmingham

    Burmingham, Alabama, United States

    Recruiting
  • University of Arkansas Medical Sciences

    Little Rock, Arkansas, United States

    Recruiting
  • Moores Cancer Center at Uc San Diego Health

    La Jolla, California, United States

    Recruiting
  • Fox Chase Cancer Center

    Philadelphia, Pennsylvania, United States

    Recruiting
  • University of Texas Southwestern

    Dallas, Texas, United States

    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
3 May 2022
Primary completion
30 Sept 2028
Completion
30 Sept 2030
Last update posted
23 Sept 2025
Registered enrollment
125
Registry id
NCT05197881

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.