Evidence map›Paper›PMID 25963327›Full record

ReviewDrugs2015

Advances in NSAID development: evolution of diclofenac products using pharmaceutical technology.

Roy Altman, Bill Bosch, Kay Brune, Paola Patrignani, Clarence Young

Registry-linked trialOpen access · hybridAbstract readReview
In one paragraph

Review in Drugs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04371549 (Skin Closures at Cesarean Delivery, Glue vs Subcuticular Sutures), which is not on this map. Cited by 137 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 2 pooled it
20.5field-weighted citation impact, top 1% 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.

NCT04371549 nacompletednot on this mapstarted 2020, after this paper: background citation

Skin Closures at Cesarean Delivery, Glue vs Subcuticular Sutures: A Randomized Clinical Trial

TypeinterventionalSponsorAin Shams Maternity HospitalRan2020 to 2021Enrolled79ConditionsCesarean Wound, DehiscenceArmsGlue (Dermabond®, Ethicon, Somerville, NJ)., Monocryl
3 · Its place in the literature

Who cites it

137 citing papers in PubMed, 2 syntheses or guidelines pooled it, 481 citations in OpenAlex.

  1. Pooled it
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  8. Simultaneous nitrogen removal and diclofenac degradation by Alcaligenes sp. FDN-09 under carbon-limited conditions.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2026
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  10. Opioidergic modulation of stress-induced hyperalgesia in adult zebrafish.Journal of neural transmission (Vienna, Austria : 1996) · 2026
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77 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 3 countries.

Roy AltmanUniversity of California, David Geffen School of Medicine, Los Angeles, CA, USA.
Bill Bosch
Kay Brune
Paola Patrignani
Clarence Young
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEiCeutica (United States) · USUniversity of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diclofenac is a nonsteroidal anti-inflammatory drug (NSAID) of the phenylacetic acid class with anti-inflammatory, analgesic, and antipyretic properties. Contrary to the action of many traditional NSAIDs, diclofenac inhibits cyclooxygenase (COX)-2 enzyme with greater potency than it does COX-1. Similar to other NSAIDs, diclofenac is associated with serious dose-dependent gastrointestinal, cardiovascular, and renal adverse effects. Since its introduction in 1973, a number of different diclofenac-containing drug products have been developed with the goal of improving efficacy, tolerability, and patient convenience. Delayed- and extended-release forms of diclofenac sodium were initially developed with the goal of improving the safety profile of diclofenac and providing convenient, once-daily dosing for the treatment of patients with chronic pain. New drug products consisting of diclofenac potassium salt were associated with faster absorption and rapid onset of pain relief. These include diclofenac potassium immediate-release tablets, diclofenac potassium liquid-filled soft gel capsules, and diclofenac potassium powder for oral solution. The advent of topical formulations of diclofenac enabled local treatment of pain and inflammation while minimizing systemic absorption of diclofenac. SoluMatrix diclofenac, consisting of submicron particles of diclofenac free acid and a proprietary combination of excipients, was developed to provide analgesic efficacy at reduced doses associated with lower systemic absorption. This review illustrates how pharmaceutical technology has been used to modify the pharmacokinetic properties of diclofenac, leading to the creation of novel drug products with improved clinical utility.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalChemistry, PharmaceuticalCyclooxygenase InhibitorsDelayed-Action PreparationsDiclofenacDose-Response Relationship, DrugHumansTechnology, PharmaceuticalAnti-Inflammatory Agents, Non-SteroidalCyclooxygenase InhibitorsDelayed-Action PreparationsDiclofenac

Identifiers

PMID25963327
PMCPMC4445819
OpenAlexW255808519

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.