NCT00324246

Feasibility Study of the NEW NORMA-SENSE

Feasibility Study of the NEW NORMA-SENSE Indicator Strip and Vaginal Secretion Buffer Capacity Measurement - IN-VITRO Study.

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 160 (actual)
• Sponsor: Carmel Medical Center · Academic / Other
• Sex: Female
• Age: 18 Years – 45 Years
• Healthy volunteers: Accepted

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

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 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.

Conditions

• Vaginal Infection

Timeline

• Start date: 2006-09-01
• Completion: 2007-12-01
• First posted: 2006-05-10
• Last updated: 2008-06-20

Locations

1 site across 1 country: Israel