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A Randomized, Double-Blind, Placebo Controlled, Parallel Assignment, Flexible Dose, Efficacy Study of Nabilone as Adjuvant in the Treatment of Diabetic Peripheral Neuropathic Pain Using an Enriched Enrollment Randomized Withdrawal Design (S38.003)

2012· article· en· W2008740860 on OpenAlexaffabout
Cory Toth, Shefina Mawani, Stefen Brady, Carmen Chan, Chin‐Chi Liu, Essie Mehina, Alexandra Garven, Jennifer Bestard, Lawrence Korngut

Bibliographic record

VenueNeurology · 2012
Typearticle
Languageen
FieldMedicine
TopicCannabis and Cannabinoid Research
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsMedicineNeuropathic painPlaceboBrief Pain InventoryRandomized controlled trialPittsburgh Sleep Quality IndexAnesthesiaPhysical therapyInternal medicineChronic painPharmacologySleep quality

Abstract

fetched live from OpenAlex

Objective: This study evaluated the oral cannabinoid, nabilone, in the treatment of refractory human diabetic peripheral neuropathic pain. Background Cannabinoids are effective for the reduction of neuropathic pain behaviours in animal models of neuropathic pain, but their efficacy in human patients is poorly established. Design/Methods: This was a single center, randomized, double blind, placebo controlled, flexible-dose study with an enriched enrollment randomized withdrawal design. Diabetic subjects with a pain score ≥4 (0–10 scale) continued their regular pain medications and were administered single blinded adjuvant nabilone for 4 weeks. Those subjects achieving ≥30% pain relief were then randomized and treated with either flexible-dose nabilone 1-4 mg/day (n = 13) or placebo (n = 13) in a further 5 week double blind treatment period. Results: Nabilone was associated with a significant improvement in the change in mean end-point pain score vs. placebo; mean treatment difference was a reduction of 1.27 (95% CI, 2.29 to 0.25) (p= 0.02). The average nabilone dose at end point was 2.9±1.1 mg/day. Nabilone was also associated with improvements from baseline when compared to placebo for the anxiety subscale of the Hospital Anxiety and Depression Scale, the Medical Outcomes Study sleep scale sleep problems index, and the European Quality of Life-5 Domains index score (each p Conclusions: Flexible-dose nabilone 1–4 mg/day was effective in relieving neuropathic pain, improvement of disturbed sleep and quality of life, and overall patient status. Nabilone was very well tolerated in patients with diabetic peripheral neuropathic pain. Larger scale studies are required to validate the use of nabilone in neuropathic pain management. Supported by: Unrestricted grant from Valeant Canada. Disclosure: Dr. Toth has received personal compensation for activities with Pfizer and Eli Lilly & Company as a speaker. Dr. Toth has received research support from Pfizer Inc, Valeant Pharmaceuticals International and Eli Lilly & Company. Dr. Mawani has nothing to disclose. Dr. Brady has nothing to disclose. Dr. Chan has nothing to disclose. Dr. Liu has nothing to disclose. Dr. Mehina has nothing to disclose. Dr. Garven has nothing to disclose. Dr. Bestard has nothing to disclose. Dr. Korngut has nothing to disclose.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.005
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.005
Threshold uncertainty score0.026

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0050.002
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0030.002
Bibliometrics0.0010.001
Science and technology studies0.0010.002
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0050.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.060
GPT teacher head0.345
Teacher spread0.285 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designRandomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2012
Admission routes2
Has abstractyes

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