New radiation method aims to reduce side effects in cervical cancer treatment
NCT ID NCT07585929
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a newer, more precise type of radiation called SBRT for women with stage IIIC cervical cancer. The goal is to see if it can safely deliver high doses to cancer in the pelvic lymph nodes while causing fewer side effects than standard radiation. About 150 women will take part, and the main focus is on tracking any serious short-term side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2024
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients with stage IIIC cervical cancer 2. No previous pelvic radiation therapy or surgery 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 Exclusion Criteria: 1. Patients with stage I or stage II or stage IV disease. 2. Patients with prior malignancies or active autoimmune diseases 3. Uncontrolled medical comorbidity
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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All India Institute of Medical Sciences
RECRUITINGDelhi, National Capital Territory of Delhi, 110049, India
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Karun Kamboj
RECRUITINGDelhi, National Capital Territory of Delhi, 110049, India
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National Cancer Institute, All India Institute of Medical Sciences, New Delhi, India
RECRUITINGNew Delhi, New Delhi, 110029, India
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a new antibody help the immune system fight Hard-to-Treat tumors?
- A simple dye might replace radioactive tracers in cancer staging
- Which radiotherapy technique offers best value for pelvic cancers?
- Enzyme-HPV link in cervical disease explored
- At-Home HPV tests could save lives of women with HIV
- Can a custom exercise plan boost survival in older women with gynecologic cancers?