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BIOEMBRACE-1

Not Applicable
Conditions
Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
Registration Number
CTRI/2019/03/018331
Lead Sponsor
Tata memorial Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) The study population will include patients recruited in the EMBRACE and EMBRACE-II studies that have completed treatment and have baseline and follow up information available.

2) Tumour sample inclusion for the molecular study necessitates that at least >40% of the sample is composed of viable tumour cells.

Exclusion Criteria

Tumour samples with less than < 40% viable tumour cells will be excluded

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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