Feasibility Study of the NEW NORMA-SENSE

Status Completed

Clinical Trial 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 capacity of vaginal secretion from non-symptomatic and symptomatic subjects

- Detect these indicator strips' performance, in contact with urine

Clinical Trial 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 elevated pH, and to measure the buffering capacity of vaginal secretion from non-symptomatic subjects and symptomatic subjects, and to detect these indicator strips' performance when come in contact with urine. ;

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective

Related Conditions & MeSH terms

Vaginal Infection

Clinical Trial Details

NCT number	NCT00324246
Study type	Observational
Source	Carmel Medical Center
Contact
Status	Completed
Phase	Phase 3
Start date	September 2006
Completion date	December 2007

View Details

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