Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age : 18 years or older Biopsy proven carcinoma cervix patients International Federation of Gynaecology and Obstetrics (FIGO) stage : stage IIIC Eastern Cooperative Oncology Group (ECOG) Performance Status Scale (PSS) 0-2 Patients who have given approval for written informed consent Patients who are eligible to receive chemotherapy
Exclusion criteria
Exclusion criteria: ECOG PSS 3-4 Post operative carcinoma cervix patients Pregnant and lactating mothers Patients who have not given approval for informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate tumour response in radiological node positive carcinoma cervix patients receiving simultaneous integrated boost along with volume based brachytherapyTimepoint: Day 1 to 15 months from start of treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| Acute bowel, bladder & rectal toxicities Late bowel ,bladder & rectal toxicities Progression free survival Overall survival Timepoint: Day 1 to 15 months after start of treatment | — |
Countries
India
Contacts
Department of Radiation Oncology ,Sri Venkateswara Institute of Medical Sciences,Tirupati