Evidence map›Paper›PMID 24220355›Full record

ArticleSexually transmitted diseases2013

Use of the dye stain assay and ultraviolet light test for assessing vaginal insertion of placebo-filled applicators before and after sex.

Marla J Keller, Niall Buckley, Lauren L Katzen, Jennifer Walsh, Barbara Friedland, Sarah Littlefield, Juan Lin, Xiaonan Xue, Terri Cornelison, Betsy C Herold and 1 more

Open access · greenAbstract read
In one paragraph

Article in Sexually transmitted diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Marla J KellerFrom the *Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY; †The Population Council, New York, NY; ‡Albert Einstein Cancer Center, Bronx, NY; and §National Cancer Institute, National Institutes of Health, Bethesda, MD.
Niall Buckley
Lauren L Katzen
Jennifer Walsh
Barbara Friedland
Sarah Littlefield
Juan Lin
Xiaonan Xue
Terri Cornelison
Betsy C Herold
Mark H Einstein
Montefiore Medical Center · USPopulation Council · USAlbert Einstein College of Medicine · USNational Institutes of Health · US

Funding

Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
Immunology/Pathology CoreP30AI051519 · NIAID · YESHIVA UNIVERSITY · PI GOLDSTEIN, HARRIS · 2003 to 2013
$18.6M
Clinical and Translational Science Award (UL1)UL1TR000086 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SHAMOON, HARRY · 2012 to 2013
$5.5M
Expanded Phase II Trial of Carraguard for Prevention of HPV InfectionR01CA148966 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI EINSTEIN, MARK H. · 2010 to 2015
$3.2M
NCATS NIH HHS UL1 TR001073NCI NIH HHS R01 CA-148966NCI NIH HHS R01 CA148966NIAID NIH HHS AI-051519NIAID NIH HHS P30 AI051519
6 · The paper itself

Abstract

backgroundApplicator dye staining and ultraviolet (UV) light have been used in trials to measure adherence, but not in the setting of before and after sex gel dosing (BAT-24). This study was designed to determine if semen or presex gel dosing impacts the sensitivity and specificity of a dye stain assay (DSA) for measuring vaginal insertion of placebo-filled applicators with BAT-24 dosing.

methodsHealthy monogamous couples received Microlax-type applicators (Tectubes, Åstorp, Sweden) filled with hydroxyethylcelluose placebo gel. Women were instructed to vaginally insert 1 dose of gel before and a second dose after sex and to return applicators within 48 hours after sex. Applicators were stained to detect semen, followed by UV then DSA, and scored by 2 readers. Positive and negative controls were randomly included in applicator batches.

resultsFifteen couples completed the study. Each woman returned at least 6 applicators over a 30-day period. The sensitivity for insertion of postsex applicators was higher for UV (97%) compared with DSA (90%), and the specificity was similar (≥96%). For presex applicators, the sensitivity and specificity were higher for DSA (100%) compared with UV testing (87% sensitivity, 96% specificity). Among returned postsex applicators, 95% tested positive by UV compared with 87% by DSA. Agreement between readers was significantly better on the presex applicators for DSA than for UV, and for postsex readings, agreement was less than half that for UV, although the results were not statistically significant.

conclusionsApplicator tests are feasible for measuring adherence in trials with gel dosing before and after sex.

Indexed as

CoitusColoring AgentsSemenUltraviolet RaysAdministration, IntravaginalAdultDrug Delivery SystemsFemaleHumansMalePatient CompliancePredictive Value of TestsReproducibility of ResultsSelf ReportSensitivity and SpecificityTime FactorsColoring Agents

Identifiers

PMID24220355
PMCPMC4143393
OpenAlexW1996685553

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.