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Efficacy and Safety of Tolperisone in Subjects With Pain Due to Acute Back Muscle Spasm

A Phase 3, 14-Day, Double-blind, Randomized, Placebo-Controlled, Multicenter Study of the Efficacy and Safety of Tolperisone in Subjects With Pain Due to Acute Back Muscle Spasm

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04671082
Acronym
RESUME-1
Enrollment
1004
Registered
2020-12-17
Start date
2020-12-15
Completion date
2022-03-21
Last updated
2022-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Pain, Back Muscle Spasm, Back Pain, Back Spasm Upper, Back Strain, Muscle Spasm

Brief summary

This is a double-blind, randomized, placebo-controlled, multicenter study of the efficacy and safety of tolperisone (a non-opioid) or placebo administered in subjects with pain due to acute back muscle spasm.

Interventions

DRUGPlacebo

TID

Sponsors

Neurana Pharmaceuticals, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Ambulatory * Current acute back pain due to acute muscle spasm starting within 7 days prior to study entry (Day 1) and at least 8 weeks following resolution of the last episode of acute back pain. * Willingness to discontinue all previous or ongoing treatment of pain or muscle spasm on study entry at Day 1 through the end of treatment including medication, acupuncture, chiropractic adjustment, massage, transcutaneous electrical nerve stimulation \[TENS\], or physiotherapy. * Pain must be localized from the neck (C-3 or lower) to the inferior gluteal folds and spasm assessed during the Screening physical examination. * Body mass index range between 18 and 35 kg/m², inclusive.

Exclusion criteria

* Presence of acute or chronic back pain for the previous 8 days or longer, where back pain is present on more days than not. * Presence of neurogenic pain in the back, neck, upper or lower extremities, including pain from (or suspected from) nerve root compression or injury (radicular pain or pinched nerve) or neuropathic pain. Evidence of these types of exclusionary pain includes radiation of pain that radiates beyond the back, chronic pain, and pain associated with abnormal sensation or loss of sensation in the back or extremities. * Presence of pain anywhere other than the target back pain that is bothersome, interferes with activity, or for which pain relief is taken. * History of any neck, back, or pelvic surgery. * History within the previous 3 years of: spinal fracture or spinal infection; inflammatory arthritis; degenerative spine disease; or any other back or spine condition that may reasonably contribute to current back pain. * Subjects who test positive for alcohol by breathalyzer test or have a positive urine drug screen for drugs of abuse (e.g. amphetamines, methamphetamines, barbiturates, benzodiazepines, cocaine, cannabinoids, oxycodone, opiates), including cannabis even where legal, at Screening.

Design outcomes

Primary

MeasureTime frameDescription
Numerical rating scale (NRS)Day 1 to Day 14Numerical rating scale (NRS), a 0-10 scale, from no pain to worst possible pain - Subject-rated pain right now due to acute back spasm.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026