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Detection of Trop2 levels and immune response against Trop2 protein in ovarian cancer patients

Not Applicable
Conditions
Health Condition 1: C569- Malignant neoplasm of unspecifiedovary
Registration Number
CTRI/2019/02/017408
Lead Sponsor
ICMR National Institute for Research in Reproductive Health
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Group A - Women with epithelial ovarian carcinoma as determined by histopathology/cytology aged 18-75 years

2.Group B - Age-matched healthy women with no reported symptoms gynecological problem (e.g. Ovarian cysts, uterine fibroids, RTI etc.)

3.Group C- Women with cervical disorder with morphologically normal ovaries undergoing hysterectomy along with oophorectomy

Exclusion Criteria

1.Group A- Non-epithelial ovarian carcinoma patients, Ovarian carcinoma patient coming with a recurrence, Patients with secondary ovarian carcinoma. Retrovirus infected patients and patients taking steroids for other disorders.

2.Group C- Cystic ovaries or ovaries with benign growth or any other significant abnormality, women with uterine endometrial disorders. Women with autoimmune disorder

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
â??To qualitatively and quantitatively measure the presence of Trop2 protein in ovarian tissue and serum of patients with epithelial ovarian cancer and healthy participantsTimepoint: Since its an observational study the time point is the first patient contact. We are not calculating statistical variables related to followup.
Secondary Outcome Measures
NameTimeMethod
To study the presence of autoantibodies and Trop2 reactive T-cells in serum of patients with ovarian cancer and healthy participantsTimepoint: Since its an observational study the time point is the first patient contact. We are not calculating statistical variables related to followup.
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