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To determine the overall survival of patients with metastatic cancer through evaluating labortory, clinical and pathological investigations.

Developing a simple outpatient prognostic score for prediction of survival in patients with advanced cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/04/008402
Enrollment
360
Registered
2017-04-24
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: null- Metastatic breast cancer OR Recurrent ovarian cancer OR Gastric/Gall bladder/Pancreatic cancer

Interventions

None listed

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Metastatic breast cancer who have received at least 2 lines of chemotherapy in metastatic setting and progressed thereafter OR 2. Recurrent ovarian cancer who have received at least 2 lines of chemotherapy for recurrent disease and progressed therafter OR 3. Gastric/Gall bladder/Pancreatic cancer patients who have received at least 1 line of chemotherapy and progressed thereafter

Exclusion criteria

Exclusion criteria: Not willing to consent for participation or not willing to be followed-up.

Design outcomes

Primary

MeasureTime frame
1. To determine the association of overall survival with various clinical, laboratory and pathological factors in patients with advanced metastatic solid cancers. 2. To create a model for predicting survival using significant variables. 3. To use the model to predict survival estimates in an independent validatory set of patients.Timepoint: Patients, satisfying the inclusion criteria and willing to participate in the study, would be recruited and prospectively followed up every 3 months (physically /telephonically) over a period of 24 months from the date of visit.

Secondary

MeasureTime frame
To build a model, using commonly available clinical, pathologic and laboratory variables, to predict survival in patients with advanced solid cancers.Timepoint: 24 months from the date of visit.

Countries

India

Contacts

Public ContactMr Yogesh Kembhavi

Tata Memorial Centre

sudeepgupta04@yahoo.com02224177201

Outcome results

None listed

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