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RECRUITING
NCT06398938

Evaluation of Ultraaccelerated High Dose Rate Intrauterine Interventional Radiotherapy

Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS

View on ClinicalTrials.gov

Summary

To evaluate the degree of acute and long-term intestinal, urinary and vaginal toxicity, and the impact on sexual activity of an accelerated fractionation of high dose rate interventional radiotherapy (IRT-HDR) in patients with locally advanced cervical cancer (IB2 - VA, N+/-).

Official title: EROS 3 Study Evaluation of Ultraaccelerated High Dose Rate Intrauterine Interventional Radiotherapy Brachytherapy in Terms of Overall Toxicity and Sexual Activity

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

129

Start Date

2024-05-06

Completion Date

2026-12-30

Last Updated

2025-08-15

Healthy Volunteers

Yes

Interventions

RADIATION

Interventional Radiotherapy

The patients will undergo four IRT fractions in one week

Locations (1)

Fondazione Policlinico Universitario A. Gemelli, IRCCS

Rome, Italy