Wallace, Andrea R., Aaron Teitelbaum, Livia Wan, Maria G.
Mulima, Laura Guichard, Stephanie Skoler, Hlengiwe Vilakazi,
Fridda S. Mapula, Jasmine Rossier, Sumen Govender, Pekka
Lähteenmäki, Robin A. Maguire, and David M. Phillips.
2007. "Determining the feasibility of utilizing the microbicide applicator
compliance assay for use in clinical trials," Contraception 76(1):
53–56. (offsite
link)
Introduction
Participants' adherence to use of study product is a major concern in
microbicide clinical trials, which can impact on proving product efficacy.
In a previously described assay, single-use microbicide applicators exposed
to the vagina were tested by spraying the applicator with trypan blue dye,
resulting in vaginal mucus staining on inserted applicators. As subjects in
our Phase 3 trials return applicators only at quarterly visits, often mixing
inserted and not-inserted applicators together in the same bag,
cross-contamination could confound results. In addition, trypan blue is
carcinogenic and thus potentially hazardous to technicians spraying daily.
Methods
Applicators that were exposed to the vagina were placed in the same bag as
unexposed applicators and shaken daily for up to 4 months. Validation was
carried out in three clinical sites in South Africa.
Results
Trypan blue was replaced with FD&C Blue #1 granular food dye.
Cross-contamination did not occur, nor did the length of time affect
reaction to dye. In South Africa, the assay was validated with an accuracy
of over 95 percent.
Conclusion
Applicator assay modifications render the test safe and suitable for use in
clinical trials.
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