Status:

COMPLETED

Feasibility Study of the NEW NORMA-SENSE

Lead Sponsor:

Carmel Medical Center

Collaborating Sponsors:

Lin Medical Center, Haifa

Common Sense

Conditions:

Vaginal Infection

Eligibility:

FEMALE

18-45 years

Brief Summary

* In-vitro study * Collect data regarding the color appearance on the new developed indicator strips (NEW NORMA-SENSE), in contact with vaginal secretion with elevated pH * Measure the buffering capac...

Detailed Description

This in-vitro study was designed to collect data regarding the color appearance on the new developed indicator strips (NEW NORMA-SENSE) when coming in contact, in-vitro, with vaginal secretion with el...

Eligibility Criteria

Inclusion

  • Women, aged between 18 and 45, with or without symptoms of vaginal infection.
  • Subjects are ready to sign the informed consent form.

Exclusion

  • Subjects are unable or unwilling to cooperate with the study procedures.
  • Subjects are currently participating in another clinical study that may directly or indirectly affect the results of this study.
  • Subjects that suffer from vaginal bleeding or menstruate.
  • Subjects that have had sexual relations within the last 12 hours.
  • Subjects that applied local antiseptic, antibiotic or vaginal treatment within the last 3 days.
  • Subjects that applied vaginal douching within 12 hours prior to the visit at the clinic.

Key Trial Info

Start Date :

September 1 2006

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 1 2007

Estimated Enrollment :

160 Patients enrolled

Trial Details

Trial ID

NCT00324246

Start Date

September 1 2006

End Date

December 1 2007

Last Update

June 20 2008

Active Locations (1)

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Women Health Care Center - Lin Medical Center

Haifa, Israel

Feasibility Study of the NEW NORMA-SENSE | DecenTrialz