Last updated: November 8, 2021
Sponsor: The Searle Company Limited Pakistan
Overall Status: Completed
Phase
N/A
Condition
Essential Tremor
Musculoskeletal Diseases
Arthritis And Arthritic Pain
Treatment
N/AClinical Study ID
NCT04765787
TSCL_NFORT-EFFECT_001
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
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
Exclusion Criteria:
- Known hypersensitivity to Nuberol Forte product, the metabolites, or formulationexcipients.
- 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 informationfor Nuberol Forte in Pakistan.
- Pregnant (assesed on LMP) or breast feeding women (assessed on interview).
Study Design
Total Participants: 399
Study Start date:
November 25, 2020
Estimated Completion Date:
August 01, 2021
Study Description
Connect with a study center
Liaquat National Hospital
Karachi, Sindh
PakistanSite Not Available
Medicare Hospital
Karachi, Sindh
PakistanSite Not Available
Patel Hospital
Karachi, Sindh
PakistanSite Not Available

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