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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02343510
Other study ID # lab7682
Secondary ID
Status Completed
Phase N/A
First received January 10, 2015
Last updated July 16, 2017
Start date January 2015
Est. completion date March 2017

Study information

Verified date July 2017
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

PCR for chlamydia DNA is done in paraffin blocks of cases of primary tubal cancer and is compared to cases of high grade serous ovarian cancer and normal tubes .


Description:

The investigators shall review the early cancer detection unite pathology records for the past 10 years , for cases diagnosed with primary Fallopian tube cancers , cases of high and low grade serous ovarian cancer and cases underwent hysterectomy and salpingectomy for non oncological reasons. Paraffin blocks for suitable selected patients will be examined histologically to confirm the primary diagnosis . Chlamydia DNA in these paraffin blocks of the Fallopian tubes and ovarian tissues will be examined using PCR techniques . The possible correlation between the presence of Chlamydia DNA and the ovarian serous tumours and primary tubal cancer will be analyzed statistically .


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date March 2017
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender Female
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- any patient with primary tubal cancer and high grade serous cancer and normal tubes.

Exclusion Criteria:

- clinical pelvic inflammatory disease

- salpingectomy for ectopic

Study Design


Related Conditions & MeSH terms


Intervention

Other:
PCR for chlamydia DNA in primary tubal cancer
PCR for presence of chlamydia DNA in paraffin blocks retrieved for tubal and ovarian tissues in all groups

Locations

Country Name City State
Egypt Ain Shams Maternity Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Presence of chlamydia DNA in tubal and ovarian tissues Up to 24 weeks
Secondary Presence of concomitant tubal cancer with high grade serous ovarian cancer Up to 8 weeks
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