Evidence map›Paper›PMID 39763591›Full record

ArticleEClinicalMedicine2024

Once daily Bromelain-based enzymatic debridement of venous leg ulcers versus gel vehicle (placebo) and non-surgical standard of care: a three-arm multicenter, double blinded, randomized controlled study.

Yaron Shoham, Robert J Snyder, Yael Katz Levy, Keren David Zarbiv, Ety Klinger, Miri Kramer, Cyaandi R Dove, Ram Avrahami, Alex Reyzelman, Felix Sigal and 17 more

Registry-linked trialAbstract read
In one paragraph

Article in EClinicalMedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03588130 (A Multicenter , Prospective, Randomized, Placebo Controlled, Adaptive Design Study Performed to Evaluate the Safety and the Efficacy of EscharEx), which is not on this map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT03588130 phase2completednot on this map

A Multicenter , Prospective, Randomized, Placebo Controlled, Adaptive Design Study Performed to Evaluate the Safety and the Efficacy of EscharEx (EX-02 Formulation) in Debridement of Venous Leg Ulcers

TypeinterventionalSponsorMediWound LtdRan2019 to 2022Enrolled120ConditionsVenous Leg UlcerArmsEscharEx (5% EX-02 formulation), Gel Vehicle, Non-surgical standard of care (NSSOC)
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. What's New in Wound Healing: Treatment Advances and Microbial Insights.American journal of clinical dermatology · 2025
    Review
  5. Review
  6. Anacaulase-Bcdb for Enzymatic Eschar Removal in Adult and Paediatric Thermal Burns: Clinical Evidence, Safety, and Therapeutic Positioning.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    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

27 authors.

Yaron ShohamDepartment of Plastic and Reconstructive Surgery, Soroka University Medical Center, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheba, Israel.
Robert J SnyderMediWound Ltd., Yavne, Israel.
Yael Katz LevyMediWound Ltd., Yavne, Israel.
Keren David ZarbivMediWound Ltd., Yavne, Israel.
Ety KlingerMediWound Ltd., Yavne, Israel.
Miri KramerMediWound Ltd., Yavne, Israel.
Cyaandi R DoveUniversity of Texas Health Science Center San Antonio, TX, USA.
Ram AvrahamiDepartment of Vascular Surgery, Rabin Medical Center, Petah Tikva, Israel.
Alex ReyzelmanDepartment of Medicine, California School of Podiatric Medicine at Samuel Merritt University, UCSF Center for Limb Preservation, San Francisco, CA, USA.
Felix SigalPodiatric Medicine, Foot and Ankle Clinic, Los Angeles, CA, USA.
Gregory TovmassianCalifornia School of Podiatric Medicine, Samuel Merritt University, San Francisco, CA, USA.
Eyal ShapiraDepartment of Plastic Surgery, Shamir Medical Center, Zerifin, Israel.
Moti HaratsDepartment of Plastic and Reconstructive Surgery, Sheba Medical Center, Tel-Hashomer, Israel.
Francisco Perez-ClavijoPodiatry Care Partners, Doral, FL, USA.
John C LantisMount Sinai West Hospital and the Icahn School of Medicine, New York, USA.
Shawn M CazzellLimb Preservation Platform, LPP Research, Fresno, CA, USA.
Yadwinder S DhillonAZ Wound/Titan Clinical Research, Phoenix, AZ, USA.
Cherison A CuffyBarry University School of Podiatric Medicine, Miami Shores, FL, USA.
Dana EgoziDepartment of Plastic and Reconstructive Surgery, Kaplan Medical Center, Rehovot, Faculty of Medicine, Hebrew University, Jerusalem, Israel.
Dean VayserDepartment of Orthopedics/Foot & Ankle Center, Scripps Clinic Medical Group, San Diego, CA, USA.
Adam J SingerDepartment of Emergency Medicine, Renaissance School of Medicine at Stony Brook University, Stony Brook, NY, USA.
Richard C GalperinMethodist Dallas Medical Center, Dallas, TX, USA.
Jason R HanftDoctors Research Network, South Miami, FL, USA.
Cindy MartinezProject 4 Research Inc., Miami, FL, USA.
Avshalom ShalomDepartment of Plastic Surgery, Meir Medical Center, Kfar Saba, Israel.
Laurence Toutous-TrelluUniversity Hospitals of Geneva, Geneva, Switzerland.
Lior RosenbergDepartment of Plastic and Reconstructive Surgery, Soroka University Medical Center, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheba, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Debridement is considered the first step in treatment of chronic wounds, however, current enzymatic and autolytic debridement agents are slow or ineffective. Previous studies have shown positive initial results with EscharEx® (EX-02 formulation), a Bromelain-based enzymatic debridement agent in development for chronic wounds. The main objective of this study was to assess its efficacy in debriding venous leg ulcers (VLU), compared to gel vehicle (GV) as a placebo control and to non-surgical standard of care (NSSOC). Methods: A prospective, randomized, multicenter, placebo-controlled trial in patients with VLU from 20 medical centers and clinics in the United States, Switzerland and Israel was undertaken. Patients were treated with daily topical applications of either EX-02, GV, or NSSOC (in a 3:3:2 ratio), until reaching complete debridement or up to 8 daily treatments (within 2 weeks), and then followed-up for up to 14 weeks. The primary efficacy endpoint was the incidence of complete debridement. This study is registered with ClinicalTrials.gov (NCT03588130) and EudraCT (number 2020-004861-38). Findings: A total of 196 patients were enrolled, and 119 randomized (between November 12th, 2019, and February 15th, 2022); 46 to the EX-02 arm, 43 to the GV arm, and 30 to the NSSOC arm. Eight patients dropped out of the study (2 in EX-02, 2 in GV, 4 in NSSOC). The incidence of complete debridement within 8 daily treatments was 63% (29/46 patients) in the EX-02 arm as compared to 30.2% (13/43 patients) in the GV arm (p = 0.004) and 13.3% (4/30 patients) in the NSSOC arm (p < 0.001). Sixty-five patients reported wound related adverse events throughout the study; 24 (52.2%), 27 (62.8%) and 14 (46.7%) patients in the EX-02, GV and NSSOC arms (p = NS). No deaths occurred during the study. Interpretation: EX-02 lead to a significantly higher incidence of complete debridement as compared to GV and NSSOC, without significant safety issues. Additional studies are needed to explore the benefits of EX-02 in VLU and other chronic wound etiologies. Funding: MediWound Ltd.

Indexed as

Chronic woundsEnzymatic debridementEscharExRCTVenous leg ulcerVLU

Identifiers

PMID39763591
PMCPMC11701486

What OpenQuestion holds

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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.