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Shorter course of radiation therapy for carcinoma of the uterine cervix using advance radiotherapy technology

Evaluation Of Acute Toxicity With Intensity Modulated Moderately Hypofractionated Whole Pelvic Radiotherapy With Image Guided High Dose Rate Brachytherapy For Locally Advanced Cervical Carcinoma - NILL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056093
Enrollment
25
Registered
2023-08-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C538- Malignant neoplasm of overlappingsites of cervix uteri

Interventions

Intervention1: Hypofractionated external beam radiotherapy to whole pelvis followed by brachytherapy: Whole pelvic hypo fractionated intensity modulated radiotherapy 40Gy in 16 fractions (2.5 Gray pe

Sponsors

Dr Ram Manohar Lohia Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Histologically proven squamous carcinoma of the uterine cervix of FIGO stage IB2-IIIC1(FIGO-2018) Patient being treated definitively with radiotherapy with or without concurrent chemotherapy. Patient willing to sign the informed consent Karnofsky Performance Status > 70 Normal complete blood counts, kidney and liver function tests No prior chemotherapy or radiotherapy and surgery

Exclusion criteria

Exclusion criteria: Stage other than IB2-IIIC1(FIGO2018) Patients who have received neoadjuvant chemotherapy. Any histopathology other than squamous cell carcinoma Synchronous or metachronous malignancy Pregnant or lactating women Uncontrolled concurrent illness like diabetes mellitus and hypertension

Design outcomes

Primary

MeasureTime frame
To assess the acute toxicity in patients of locally advanced cervical carcinoma treated with hypo fractionated intensity modulated radiotherapy followed by high dose rate brachytherapyTimepoint: Weekly during treatment, monthly for the first 3 months, then 2 monthly for the next 6 months & then 3 monthly until 2 year after treatment.

Secondary

MeasureTime frame
To assess the late toxicity & early clinical outcome in terms of loco-regional control at six months for this regimen Timepoint: 2 years from the completion of treatment

Countries

India

Contacts

Public ContactDr Siddharth Burman

Dr Ram Manohar Lohia Institute of Medical Sciences

ajeetgandhi23@gmail.com8176007283

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026