NFORT-EFFECT: Safety & Efficacy of Nuberol Forte® in Pain Management

Sponsor
The Searle Company Limited Pakistan (Industry)
Overall Status
Completed
CT.gov ID
NCT04765787
Collaborator
(none)
399
3
8.2
133
16.3

Study Details

Study Description

Brief Summary

The global prevalence of Musculoskeletal disorders (MSD) ranges from 14% to as high as 42%. In addition WHO also estimates that 40% of people over the age of 60 years suffer from MSD and about 80% of the people have had low back pain at some point in their life. In Pakistan, to estimate the prevalence of MSD, there is no data available based on the local population. Locally, studies were conducted on the specific subject pools mainly considering the work related musculoskeletal disorders and backache. However, no real data is available for the symptomatic management of painful musculoskeletal disorders in multiple settings to calculate more generalizable results. So this study is planned and if we found good results then it will help physicians to prescribe the above said medicine to all such cases.

Condition or Disease Intervention/Treatment Phase
  • Drug: Combination of Paracetamol 650mg + Orphenadrine 50mg

Detailed Description

The management of musculoskeletal pain is complex therefore plethora of treatment options are available include non-pharmacological treatments , complementary therapies, and pharmacological interventions. In order to provide optimal care to patients with musculoskeletal pain and ensure the efficient use of healthcare resources, a comprehensive overview of the available evidence for the most effective treatment options for musculoskeletal pain presentations is essential. In this context, an observational study is planned on the efficacy and safety of analgesic combination (i.e Nuberol Forte®). Nuberol Forte® is a combination of muscle relaxant (Orphanedrine) and an analgesic/antipyretic (Paracetamol/Acetaminophen). There are clear indications that the combination of Orphenadrine with Paracetamol may give increased antinociceptive activity and duration of action over and above the use of Orphenadrine or Paracetamol alone.

Study Design

Study Type:
Observational
Actual Enrollment :
399 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Clinical Response of Nuberol Forte® for the Pain Management in Musculoskeletal Disorders in Routine Pakistani Practice
Actual Study Start Date :
Nov 25, 2020
Actual Primary Completion Date :
Apr 1, 2021
Actual Study Completion Date :
Aug 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Painful musculoskeletal disorders in random order

Nuberol Forte® (Paracetamol 650 mg + Orphenadrine 50 mg) for the symptomatic management of the painful musculoskeletal disorders one tablet three times a day or as per physician discretion or as per severity of pain and treatment duration is 7-10 days

Drug: Combination of Paracetamol 650mg + Orphenadrine 50mg
In routine practice for pain , combination of Paracetamol 650 mg + Orphenadrine 50mg prescribed for 7-10 days with follow up and as per physician discretion
Other Names:
  • Nuberol Forte
  • Outcome Measures

    Primary Outcome Measures

    1. To assess the effectiveness of Nuberol Forte from baseline to 2 weeks [2 weeks]

      the pain, muscle spasm and stiffness are assessed by Muscle & Joint Measure scale.

    2. To assess the safety of Nuberol Forte in the cases presenting with Musculoskeletal disorder [2 weeks]

      Safety is monitored from the first dose of the study drug

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient with a clinical history of painful musculoskeletal disorder from last 1 year

    • Patient aged ≥18 and ≤70 years inclusive of either sex

    • Patient with ability to understand and sign written informed consent form.

    Exclusion Criteria:
    • Known hypersensitivity to Nuberol Forte product, the metabolites, or formulation excipients.

    • Patients with Glaucoma, prostatic hypertrophy or obstruction at the bladder neck, myasthenia gravis, oesophageal spasm and pyloric or duodenal obstruction.

    • Treated with Nuberol Forte to evaluate safety as per approved prescribing information for Nuberol Forte in Pakistan.

    • Pregnant (assesed on LMP) or breast feeding women (assessed on interview).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Liaquat National Hospital Karachi Sindh Pakistan
    2 Medicare Hospital Karachi Sindh Pakistan
    3 Patel Hospital Karachi Sindh Pakistan

    Sponsors and Collaborators

    • The Searle Company Limited Pakistan

    Investigators

    • Study Director: Asif Mahmood, Dr., The Searle Company Limited

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    The Searle Company Limited Pakistan
    ClinicalTrials.gov Identifier:
    NCT04765787
    Other Study ID Numbers:
    • TSCL_NFORT-EFFECT_001
    First Posted:
    Feb 21, 2021
    Last Update Posted:
    Nov 10, 2021
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by The Searle Company Limited Pakistan
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 10, 2021