DANTE Study: The First Randomized, Double-Blind, Placebo and Active-Controlled, Parallel Arm Group Study Evaluating the Analgesic Efficacy and Safety of Dexketoprofen TrometAmol aNd Tramadol Hydrochloride Oral FixEd Dose Combination on Moderate to Severe Acute Pain in Patients with Acute Low Back Pain-Rationale and Design

Giustino Varrassi; Magdi Hanna; Stefano Coaccioli; Meto Suada; Serge Perrot

doi:10.1007/s40122-022-00407-8

DANTE Study: The First Randomized, Double-Blind, Placebo and Active-Controlled, Parallel Arm Group Study Evaluating the Analgesic Efficacy and Safety of Dexketoprofen TrometAmol aNd Tramadol Hydrochloride Oral FixEd Dose Combination on Moderate to Severe Acute Pain in Patients with Acute Low Back Pain-Rationale and Design

Pain Ther. 2022 Sep;11(3):1055-1070. doi: 10.1007/s40122-022-00407-8. Epub 2022 Jul 5.

Authors

Giustino Varrassi¹, Magdi Hanna², Stefano Coaccioli³, Meto Suada⁴, Serge Perrot⁵

Affiliations

¹ Paolo Procacci Foundation, Via Tacito 7, 00193, Rome, Italy. giuvarr@gmail.com.
² Analgesics and Pain Research (APR) Ltd, Beckenham, UK.
³ European League Against Pain, Zurich, Switzerland.
⁴ Global Medical Affairs, Menarini, Florence, Italy.
⁵ Pain Center, INSERM U987, Hôpital Cochin, University of Paris, Paris, France.

Abstract

Introduction: Despite a wide range of treatment approaches and the availability of treatment recommendations or guidelines, no consensus on the most effective pharmacological therapy of low back pain (LBP) has been reached yet. Therefore, additional clinical evidence, particularly if built upon a rigorous clinical trial design, an evidence-based medication choice, and broader inclusion criteria better acknowledging the heterogeneity and intrinsic variability of LBP is needed. The DANTE study has been designed to comprehensively assess the analgesic efficacy and tolerability of dexketoprofen/tramadol (DKP/TRAM) 75/25 mg in a large cohort of patients with moderate to severe acute LBP.

Methods: The DANTE study is a phase IV, multicenter, randomized, double-blind, double-dummy parallel group, placebo, and active controlled study. The DANTE study encompasses a single-dose phase (day 1, t0-t8h) and a multiple-dose phase (from t8h to 8 h after intake of last dose at day 5). The DANTE study population includes patients naïve to LBP or patients with previous history of LBP experiencing a new episode of moderate to severe intensity with or without radiculopathy. The clinical phase of the DANTE study started in September 2020 and the anticipated completion date is April 2022.

Planned outcomes: The primary endpoint is the time to first achieve a numeric rating scale-pain intensity (NRS-PI) score of < 4 or a pain intensity reduction ≥ 30% from drug intake up to 8 h after the first dose (t8h). Secondary objectives aim are: (1) to evaluate the analgesic efficacy of TRAM/DKP 75/25 mg versus TRAM 100 mg after the first dose; (2) to evaluate the analgesic efficacy of TRAM/DKP 75/25 mg versus TRAM 100 mg after the multiple doses (from t8h until day 5, multiple dose); and (3) to assess the safety and tolerability of the TRAM/DKP 75/25 mg fixed combination after single and multiple doses.

Dante study registration: EudraCT number: 2019-003656-37.

Keywords: Acute pain; Dexketoprofen; Low back pain; Radiculopathy; Tramadol.