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OncoMatch/Clinical Trials/NCT07625943

HYPOfractionated RadioTherapy in Cervical Cancer

Is NCT07625943 recruiting? Yes, currently enrolling (Jul 2026). This NA trial studies non-drug interventions for cervical cancer squamous cell.

NARecruitingAll India Institute of Medical SciencesNCT07625943Data as of Jul 2026Location: India

The study is a prospective, randomized, non-inferiority clinical trial which will test whether a short course of radiation treatment (hypofractionation) for cervical cancer works as well as the standard longer course. Cervical cancer is one of the most common cancers in women in India, and many patients have trouble completing treatment because it takes several weeks and requires many hospital visits. In this trial, females with locally advanced cervical cancer will be randomly assigned to one of two treatment groups. One group will receive the standard radiation schedule with External Beam RadioTherapy (EBRT) over about 5 weeks, weekly cisplatin chemotherapy, and brachytherapy. The other group will receive a shorter, hypofractionated external beam radiotherapy schedule over about 3 weeks, the same chemotherapy, and brachytherapy. Researchers will compare the two groups to see whether the hypofractionated schedule is non-inferior to the standard radiation therapy schedule. The main outcomes will be tumor control in the pelvis, side effects, survival, and quality of life. If the hypofractionated schedule meets the non-inferiority limit, it could reduce treatment time, improve patient convenience, and help more people receive treatment in busy cancer centers in emerging countries.

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Extracted eligibility criteria

Cancer type

Cervical Cancer

Disease stage

Required: Stage II, IIIA, IIIB, IIIC1

Excluded: Stage IIIC2, IVA, IVB

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 65
Female only

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: pelvic radiotherapy

Cannot have received: chemotherapy for cervical cancer

Lab requirements

Blood counts

adequate hematological function

Kidney function

adequate renal function

Liver function

adequate hepatic function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07625943 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

What disease stage is eligible?

Stage II or IIIA or IIIB or IIIC1 is required.

Is there an age limit?

Yes. Patients must be 65 years or younger.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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