Evidence map›Paper›PMID 33219482›Full record

Trial reportArchives of gynecology and obstetrics2021

Efficacy and safety of an adsorbent and anti-oxidative vaginal gel on CIN1 and 2, on high-risk HPV, and on p16/Ki-67: a randomized controlled trial.

Attila Louis Major, Vladimír Dvořák, Jana Schwarzová, Aleš Skřivánek, Tomáš Malík, Marek Pluta, Ivanna Mayboroda, Etienne Marc Grandjean

Erratum issued Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Archives of gynecology and obstetrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05509413 (DEFLAGYN® Vaginal Gel and Spontaneous Remission and Regression of Unclear Cervical Smears and HPV High-risk Infections), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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.

NCT05509413 nacompletednot on this mapstarted 2022, after this paper: background citation

DEFLAGYN® Vaginal Gel and Spontaneous Remission and Regression of Unclear Cervical Smears and HPV High-risk Infections

TypeinterventionalSponsorRuhr University of BochumRan2022 to 2025Enrolled242ConditionsCervix Dysplasia, HPV InfectionArmsDEFLAGYN vaginal gel
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 3 countries.

Attila Louis MajorFemina Gynecology Center, Rue Emile-Yung 1, 1205, Geneva, Switzerland. majorattila@outlook.fr.ORCID 0000-0002-1459-2727
Vladimír DvořákCentrum ambulantní Gynekologie a primární péče, s.r.o., Brno, Czech Republic.
Jana Schwarzová, Smetanova 388, 252 64 Velké Prilepy, Prague-West, Czech Republic.
Aleš SkřivánekG-CENTRUM Olomouc, s.r.o., Olomouc, Czech Republic.
Tomáš MalíkGyneko spol. s.r.o., Vsetin, Czech Republic.
Marek PlutaFakultní Nemocnice v Motole (University Hospital Motol), Onkogynekologická a kolposkopická Ambulance, Praha, Czech Republic.
Ivanna MayborodaDepartment of Obstetrics and Gynecology, University Hospital of Geneva, Geneva, Switzerland.
Etienne Marc GrandjeanPhidalsa Pharma-Consultants, Petit-Lancy/Geneva, Switzerland.
Food Research Institute Prague · CZMolecular Partners (Switzerland) · CHUniversity Hospital in Motol · CZUniversity Hospital of Geneva · CHUniversity of Fribourg · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe effect of SAM vaginal gel, a medical device containing adsorptive silicon dioxide and antioxidative sodium selenite and citric acid, on histologically-proven cervical intraepithelial neoplasia type 2 (CIN2) as well as p16 positive CIN1, and on the presence of the onco-marker p16 was investigated.

methods216 women aged 25-60 years were randomized to either receive an intravaginal daily dose of SAM gel for three 28-day periods, or be followed-up without intervention. The primary endpoint was efficacy, defined as a combined histological and cytological regression. At baseline and after 3 months participants had: a guided biopsy including p16 immunohistochemical (IHC) staining, only if a lesion was visible at colposcopy; a cervical smear for cytology, high-risk human papillomavirus (hr-HPV) and a p16/Ki-67 test. At 6 months a further cytology and p16/Ki-67 test was performed.

resultsRegression of CIN lesions was observed in 78 out of 108 patients (72.2%) in the SAM gel arm and in 27 out of 108 patients (25.0%) in the control arm. Similarly, the change in the p16/Ki-67 cytological test status was significantly in favor of the treatment arm. The prevalence of hr-HPV decreased significantly (p < 0.001) in the treatment arm, from 87.0% to 39.8%, while it slightly increased in the control arm, from 78.7% to 83.3%. At 6 months the cytological regression in the treatment group and the highly significant effect on p16/Ki-67 was still present.

conclusionSAM vaginal gel enhances the regression of cervical lesions and clears hr-HPV and p16/Ki-67 in smears significantly, thus offering an active non-destructive management to prevent cervical cancer. TRIAL REGISTRATION NUMBER: ISRCTN11009040, date of registration: 10/12/2019; https://doi.org/10.1186/ISRCTN11009040 ; retrospectively registered.

Indexed as

Vaginal Creams, Foams, and JelliesAdministration, IntravaginalAdultAntioxidantsBiomarkers, TumorCitric AcidColposcopyCyclin-Dependent Kinase Inhibitor p16CytodiagnosisFemaleGenes, p16HumansKi-67 AntigenMiddle AgedPapillomavirus InfectionsPregnancyAntioxidantsBiomarkers, TumorCitric AcidCyclin-Dependent Kinase Inhibitor p16Ki-67 AntigenSilicon DioxideSodium SeleniteVaginal Creams, Foams, and JelliesCervical intraepithelial neoplasiaHPVNon-surgical treatmentp16/Ki-67 dual stainingSilicon dioxideSodium selenite

Identifiers

PMID33219482
PMCPMC7858556
OpenAlexW4238787293

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.