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Completed

NCT Number: NCT02865161

Amtolmetin Gaucil in Knee Osteoarthritis

This study is conducted to study the efficacy and safety of Niselat in patients with osteoarthritis.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

About this study

Osteoarthritis is the most common rheumatic disease. Knee OA (KOA), gonarthrosis (GA), is characterized by high prevalence, progressive course with early disability of the subject, persistent pain syndrome for the treatment of which non-steroidal anti inflammatory drugs (NSAIDs) are actively used in clinical practice. It was revealed that NSAIDs may cause gastrointestinal adverse effects (AEs), from mild dyspepsia to bleeding and perforation as well as cardiovascular effects. Gastroprotection with misoprosol, Н2-receptor antagonists and proton pump inhibitors (PPI) is not always effective. NSAIDs with the lowest gastrointestinal toxicity with efficacy adequate to suppress joint pain is justified and reasonable.

Amtolmetin guacil (AMG) is a new NSAID which proved to be the least gastrointestinally toxic in experimental studies in vivo, in vitro and in comparative clinical studies. AMG does not have selectivity towards COX-2 or NO. AMG exerts gastroprotective effect due to stimulation of capsaicin receptors (vanilloid receptors) in gastrointestinal wall. To assess tolerability of amtolmetin guacil, it is first necessary to obtain data on potential reduction of dyspeptic symptoms including in subjects with these signs of NSAIDs intolerability.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent form for participation in the study;
  • KOA (based on ACR, 1987)
  • Age between 30-60 years old
  • Previous regular administration of NSAIDs for at least 4 weeks (at maximum therapeutic dose)
  • Dyspeptic symptoms (according to SODA questionnaire)
  • Pain intensity in the investigated knee joint ≥ 40 mm according to VAS
  • Subjects with systolic blood pressure ≤ 140 mm Hg and diastolic BP ≤90 mmHg against stable antihypertensive therapy.

Exclusion criteria

  • Contraindications to amtolmetin guacil (according to patient information leaflet)
  • Subjects with SBP ≥140 mm Hg and DBP ≥90 mm Hg
  • Signs of renal or hepatic failure;
  • Pregnancy, lactation or planning for pregnancy.
  • One of the following changes in laboratory values at screening HGB, WBC, ESR, ALT, AST.

Treatment and study plan

NISELAT

Drug

NISELAT 600MG BD

Other names: AMTOLMETIN GAUCIL

Primary outcomes

  1. Reduction in WOMAC score from baseline

    Time frame: Baseline to 4 weeks

    Reduced WOMAC (according to pain, rigidity and function scales) by > 20 % vs. baseline.

Secondary outcomes

  1. Change in VAS

    Time frame: Baseline to 45 weeks

  2. SODA Questionnaire

    Time frame: Baseline to 4weeks

  3. No of adverse events

    Time frame: Baseline to 4 week

    Total number of adverse events

Sponsors and collaborators

Lead sponsor

Dr. Reddy's Laboratories Limited

Industry

Registry information

Official study title

Open-label, Multicenter, Observational (Non-interventional) Study of Efficacy and Tolerability of Amtolmetin GuAcil in Subjects With Knee osTeoArthrosis With Dyspepsia. (AGATA)

Acronym: AGATA

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Aug 12, 2016
Registry last updated
Sep 30, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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