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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04067557
Other study ID # BV
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2013
Est. completion date June 1, 2013

Study information

Verified date August 2019
Source Skaraborg Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Among 300 women that are scheduled a therapeutic abortion screening diagnopsis of BV are done using Gram stained vaginal smear and with a molecular test using PCR for 5 different bacteria.


Description:

The molecular test will test for Atophobium vaginae, Leopitrichia spp, Megasphaera Mobiluncus and BVAB2


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date June 1, 2013
Est. primary completion date May 1, 2013
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

women scheduled a therapeutic abortion (Before 12th week) will be screened for gential infections such as chlamydia and Gc together with bacterial vaginosis

Exclusion Criteria:

- women not pregnat

Study Design


Intervention

Diagnostic Test:
molecuar test of BV
diagnosis of BV

Locations

Country Name City State
Sweden Department of Ob/Gyn, Skaraborgshospital Skövde Skövde

Sponsors (1)

Lead Sponsor Collaborator
Skaraborg Hospital

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnosis of bacterial vaginosis comparing modified Hay/Ison with molecular diagnosis Comparing the Gram stained vaginal smears using Hay/Ison (i.e. BV or normal) criteria with a molecular PCR method with 5 different bacterium and after an algoritm end up with the result (i.e. BV or normal). The number of women with the diagnosis of BV with each of the diagnostic test can be compared calculatitng a KAPPA index 4 month
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