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Study of checking if plan made in treatment machine of Radiotherapy is equivalent to plan made in planning CT

Simulation Omitted Radiotherapy SORT for External Beam Boost in cervical cancer patients A feasibility study from a tertiary care center in India - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/07/114206
Enrollment
10
Registered
2026-07-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

Mahamana Pandit Madan Mohan Malaviya Cancer Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of cancer cervix FIGO stage IB3 to IVA 2. Age greater than or equal to 18 years 3. Patient has undergone EBRT with a dose of 45 to 50Gy to the cervix and draining lymph nodes 4. Post EBRT deemed not fit for brachytherapy

Exclusion criteria

Exclusion criteria: 1. Cancer cervix treated with palliative intent 2. Patients fit for brachytherapy 3. Post operative cancer cervix patients

Design outcomes

Primary

MeasureTime frame
Evaluate the feasibility of SORT protocol for treating cancer cervix patients unfit for Brachytherapy 2. Evaluate the validity of SORT plans by performing dosimetric comparison with conventional plansTimepoint: 6 months

Secondary

MeasureTime frame
Couch shifts pattern & uterine movement with adequacy of PTV marginsTimepoint: 5 days;Acute & late treatment related toxicityTimepoint: 6 months;Local control LC and volumetric assessment of OARsTimepoint: At 6 months post treatment

Countries

India

Contacts

Public ContactDr Avradeep Datta

Mahamana Pandit Madan Mohan Malaviya Cancer Centre Unit of Tata Memorial Centre, Varanasi

avradeepd@mpmmcc.tmc.gov.in6283322872

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026