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Patterns Of Haematological Biomarker in cervical cancer patients and its association with its covariates

Not Applicable
Conditions
Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
Registration Number
CTRI/2023/06/053636
Lead Sponsor
Vardhman Mahavir Medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients with positive biopsy report of cervical carcinoma at any stage of the disease

Exclusion Criteria

Patients who donâ??t have a record of their Pre Treatment Neutrophil lymphocyte Ratio (NLR).

Severely ill patients not able to converse.

Patients suffering from sepsis.

Patients with a positive biopsy for blood cancer.

Patients with a history of tuberculosis.

Patients with severe wounds.

Any other severe inflammation except cervical cancer.

Patients with active liver disease, including those with primary biliary cirrhosis and unexplained persistent liver function abnormalities.

Any medication or indication that may interfere with the interpretation of study results and, in the judgment of the study personnel, would make the subject inappropriate for inclusion.

Patients with history of severe allergies.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To find mean Neutrophil Lymphocyte Ratio(NLR) among cervical cancer patients.Timepoint: 9 weeks
Secondary Outcome Measures
NameTimeMethod
To check association of Neutrophil Lymphocyte Ratio(NLR) with Sociodemographic, lifestyle & reproductive factors among cervical cancer patients.Timepoint: 9 weeks;To compare Neutrophil Lymphocyte Ratio(NLR) among various stages of cervical cancer.Timepoint: 9 weeks
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