Evidence map›Paper›PMID 27052991›Full record

Trial reportTrials2016

A clinical trial comparing Lanconone® with ibuprofen for rapid relief in acute joint pain.

Robert N Girandola, Shalini Srivastava, Costas C Loullis

2 registry-linked trialsOpen access · goldAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Trials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 31% 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.

NCT02417506 nacompletednot on this map

A Double Blind Randomized Comparator Controlled Study to Assess the Effect of E-OA-07 (Lanconone) on Acute Pain Response in Subjects Suffering From Osteoarthritis of the Knee

TypeinterventionalSponsorVedic Lifesciences Pvt. Ltd.Ran2014 to 2015Enrolled72ConditionsOsteoarthritis of KneeArmsE-OA-07 (Lanconone), Ibuprofen
NCT03262805 nacompletednot on this mapstarted 2017, after this paper: background citation

To Assess the Lanconone® (E-OA-07) Efficacy in Physical Activity-related Pain- LEAP Study

TypeinterventionalSponsorVedic Lifesciences Pvt. Ltd.Ran2017 to 2018Enrolled73ConditionsKnee OsteoarthritisArmsLanconone, Placebo
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

3 authors at 1 institution in 1 country.

Robert N GirandolaDepartment of Biological Sciences, University of Southern California, Greater Los Angeles, CA, USA.
Shalini SrivastavaResearch & Development, Enovate Biolife, Wilmington, DE, USA. shalini@enovatebiolife.com.
Costas C LoullisANIXIS Biomedical Consulting, Chapel Hill, NC, USA.
University of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo study the effect of Lanconone® (1000 mg) on acute pain on exertion as compared to the standard of care, Ibuprofen (400 mg).

methodThe study recruited 72 subjects diagnosed with mild to moderate knee joint pain on exertion. Subjects with Pain Visual Analogue Scale of more than 40 mm were included. Uphill walking was provided as the stressor using Naughton's protocol on a treadmill. The subjects walked for 10 minutes continuously followed by a rest period and baseline pain score for index knee joint was recorded. Subjects were administered a single dose of Lanconone® (1000 mg)/Ibuprofen (400 mg). Thereafter the same stressor was provided at 0.5, 1, 2, 3, 4, and 6 hours, subsequently, pain scores were recorded on a visual analogue scale. Double stopwatch method was used to evaluate the onset of pain relief and time taken to meaningful pain relief.

resultBoth Lanconone® and Ibuprofen showed the first perceived pain relief at 65.31 ± 35.57 mins as compared to 60.82 ± 32.56 mins respectively. The mean time taken to experience meaningful pain relief in Lanconone® group was 196.59 ± 70.85 mins compared to 167.13 ± 71.41 mins amongst Ibuprofen group. The meaningful pain relief continued for 6 hours.

conclusionThe current study successfully demonstrated rapid pain-relieving potential of Lanconone® which was comparable to Ibuprofen. No adverse event related to the interventions was reported in the study.

trial registrationClinical trials.gov NCT02417506 . 21 January 2015.

Indexed as

Acute PainAdultAnalgesicsAnti-Inflammatory Agents, Non-SteroidalArthralgiaDouble-Blind MethodExercise TestFemaleHumansIbuprofenKnee JointMaleMiddle AgedPain MeasurementPain PerceptionPlant ExtractsAnalgesicsAnti-Inflammatory Agents, Non-SteroidalIbuprofenPlant ExtractsAnalgesicArthritisGlucosamineHealth supplementIbuprofenJoint painNonsteroidal anti-inflammatory drugRapid pain reliefTraumaVisual analogue scale

Identifiers

PMID27052991
PMCPMC4823836
OpenAlexW2317006557

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.