Evidence map›Paper›PMID 25703647›Full record

Trial reportWound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society

Topical administration of a connexin43-based peptide augments healing of chronic neuropathic diabetic foot ulcers: A multicenter, randomized trial.

Christina L Grek, G M Prasad, Vijay Viswanathan, David G Armstrong, Robert G Gourdie, Gautam S Ghatnekar

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
6.9field-weighted citation impact, top 2% 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

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

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  14. Degradation of the α-Carboxyl Terminus 11 Peptide:ACS pharmacology & translational science · 2024
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3 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

6 authors at 5 institutions in 2 countries.

Christina L GrekFirstString Research, Inc., Mount Pleasant, South Carolina.
G M PrasadPace Clinical Research Center, Bangalore, Karnataka, India.
Vijay ViswanathanM.V. Diabetes and Research Center, Chennai, Tamil Nadu, India.
David G ArmstrongSouthern Arizona Limb Salvage Alliance (SALSA), Department of Surgery, University of Arizona College of Medicine, Tucson, Arizona.
Robert G GourdieVirginia Tech Carilion Research Institute, Center for Heart and Regenerative Medicine Research, Roanoke, Virginia.
Gautam S GhatnekarFirstString Research, Inc., Mount Pleasant, South Carolina.
FirstString Research (United States) · USBangalore Diabetes Centre · INCarilion Clinic · USM.V. Hospital for Diabetes and Diabetes Research Centre · INUniversity of Arizona · US

Funding

Evaluation Of A Novel Connexin-Based Peptide For The Treatment Of Diabetic WoundsR44DK080567 · NIDDK · XEQUEL BIO, INC. · PI GHATNEKAR, GAUTAM SUDHIR · 2010 to 2016
$3.9M
Evaluation of a novel connexin-based peptide for the treatment of diabetic woundsR43DK080567 · NIDDK · XEQUEL BIO, INC. · PI GHATNEKAR, GAUTAM SUDHIR · 2007 to 2007
$141k
NIDDK NIH HHS 1R43DK080567-01NIDDK NIH HHS 2R44 DK080567 -02NIDDK NIH HHS R43 DK080567NIDDK NIH HHS R44 DK080567
6 · The paper itself

Abstract

Nonhealing neuropathic foot ulcers remain a significant problem in individuals with diabetes. The gap-junctional protein connexin43 (Cx43) has roles in dermal wound healing and targeting Cx43 signalling accelerates wound reepithelialization. In a prospective, randomized, multicenter clinical trial we evaluated the efficacy and safety of a peptide mimetic of the C-terminus of Cx43, alpha connexin carboxy-terminal (ACT1), in accelerating the healing of chronic diabetic foot ulcers (DFUs) when incorporated into standard of care (SOC) protocols. Adults with DFUs of at least four weeks duration were randomized to receive SOC with or without topical application of ACT1. Primary outcome was mean percent ulcer reepithelialization and safety variables included incidence of treatment related adverse events (AEs) and detection of ACT1 immunogenicity. ACT1 treatment was associated with a significantly greater reduction in mean percent ulcer area from baseline to 12 weeks (72.1% vs. 57.1%; p = 0.03). Analysis of incidence and median time-to-complete-ulcer closure revealed that ACT1 treatment was associated with a greater percentage of participants that reached 100% ulcer reepitheliazation and a reduced median time-to-complete-ulcer closure. No AEs reported were treatment related, and ACT1 was not immunogenic. Treatment protocols that incorporate ACT1 may present a therapeutic strategy that safely augments the reepithelialization of chronic DFUs.

Indexed as

Adaptor Proteins, Signal TransducingAdministration, TopicalAnti-Infective AgentsConnexin 43Diabetic FootFemaleHumansMaleMiddle AgedPeptidesProspective StudiesSurgical Wound InfectionTreatment OutcomeTumor Necrosis Factor Receptor-Associated Peptides and ProteinsWound HealingAdaptor Proteins, Signal TransducingAnti-Infective AgentsConnexin 43PeptidesTRAF3IP2 protein, humanTumor Necrosis Factor Receptor-Associated Peptides and Proteins

Identifiers

PMID25703647
PMCPMC4472499
OpenAlexW1702382101

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.