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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01688258
Other study ID # GUD-PCR
Secondary ID
Status Completed
Phase N/A
First received September 14, 2012
Last updated July 12, 2017
Start date January 2012
Est. completion date July 2013

Study information

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

Clinical Trial Summary

(i) To compare a new diagnostic PCR with established diagnostic procedures for T. pallidum (serology, dark field microscopy), H. ducreyi (cultivation), HSV types 1 and 2 (cultivation, PCR).

(ii) To assess the frequency of infections with T. pallidum, H. ducreyi and HSV types 1 and 2 in patients with genital, anal and oropharyngeal ulcers by a new PCR.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date July 2013
Est. primary completion date July 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion criteria:

- Patient with genital, anal or oropharyngeal ulcers

- Age minimum of 18 years.

- Informed consent must be obtained from each patient/control patient in written form prior to any study procedure.

Exclusion criteria:

- Antibiotic therapy within 2 weeks before the visit

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Diagnostic swab


Locations

Country Name City State
Switzerland University Hospital Zurich, Division of Dermatology Zurich ZH

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland,