Evidence map›Paper›PMID 26268443›Full record

Trial reportEuropean journal of clinical pharmacology2015

Iontophoresis driven concentrations of topically administered diclofenac in skeletal muscle and blood of healthy subjects.

Richard Crevenna, Angela Burian, Zoe Oesterreicher, Edith Lackner, Walter Jäger, Gottfried Rezcicek, Mohammad Keilani, Markus Zeitlinger

Abstract readClinical Trial
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In one paragraph

Trial report in European journal of clinical pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 2 institutions in 1 country.

Richard CrevennaDepartment of Physical Medicine and Rehabilitation, Medical University Vienna, Vienna, Austria.
Angela BurianDepartment of Physical Medicine and Rehabilitation, Medical University Vienna, Vienna, Austria.
Zoe OesterreicherDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Edith LacknerDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Walter JägerDepartment of Clinical Pharmacy and Diagnostics, University of Vienna, Vienna, Austria.
Gottfried RezcicekDepartment of Pharmacognosy, University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Mohammad KeilaniDepartment of Physical Medicine and Rehabilitation, Medical University Vienna, Vienna, Austria.
Markus ZeitlingerDepartment of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria. markus.zeitlinger@medunivie.ac.at.
Medical University of Vienna · ATUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe present open single-centre, descriptive and comparative pharmacokinetic study aimed to investigate the efficacy of iontophoresis to enhance transdermal delivery by measuring concentration vs. time profiles of diclofenac in local tissue and in plasma in two separate study periods.

methodsPeriod 1 determined diclofenac concentrations in both calf muscles simultaneously by using microdialysis after applying diclofenac gel topically as a single dose of 5 g with or without iontophoresis in eight healthy volunteers. In period 2, the same dose was applied to another 8 volunteers to determine plasma concentrations of diclofenac either with or without iontophoresis in a cross over design.

resultsIn period 1, tissue concentrations were found to be under the limit of detection of 0.5 ng/ml both with and without iontophoresis in all subjects. In period 2, after iontophoresis in 75% of study participants, plasma concentrations of diclofenac could be determined, but only in 25% without iontophoresis. Although area under the concentration-time-curve (AUC, 187.97 ± 315.92 vs. 22.92 ± 42.44 ng*min/ml) and maximum concentration (Cmax, 2.06 ± 3.79 vs. 0.22 ± 0.41 ng/ml) values showed a numerically clear trend for higher values with iontophoresis compared to passive diffusion, no significant difference could be found due to high inter-individual variability. In total, 18.75% of all subjects presented adverse events.

conclusionsDespite a higher percentage of subjects showed detectable plasma levels of diclofenac after iontophoresis, iontophoresis failed to achieve potentially more effective topical concentrations. The typical mechanism of iontophoresis like electromigration, electroosmosis and increased subcutaneous circulation could be responsible for the results of the present observation. Additional clinical studies are needed to justify the transdermal delivery of diclofenac by using iontophoresis.

Indexed as

IontophoresisAdministration, TopicalAnti-Inflammatory Agents, Non-SteroidalDiclofenacHealthy VolunteersHumansMaleMuscle, SkeletalAnti-Inflammatory Agents, Non-SteroidalDiclofenacDiclofenacIontophoresisMicrodialysisPharmacokinetics

Identifiers

PMID26268443
OpenAlexW1177413664

What OpenQuestion holds

Textmetadata
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.