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Influence of drug containing ginger extract on arthritic pain and gastropathy in patients with osteoarthritis

Influence of drug containing ginger extract on arthritic pain and gastropathy in patients with osteoarthritis: a randomised active controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN48110500
Enrollment
40
Registered
2010-11-26
Start date
2008-06-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Osteoarthritis, NSAID-induced gastropathy Musculoskeletal Diseases Osteoarthritis

Interventions

The patients were randomised in two groups, using methods of envelopes, to: 1. Group ZG (n = 21): ginger and glucosamine combination (Zinaxin Glucosamine: 170 mg ginger extract [Zingiber officinalis,

Sponsors

Central Scientific Research Institute of Gastroenterology (Russia)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years, either sex 2. Osteoarthritis (OA) pain syndrome availability of more than 40 mm according to Visual Analogue Scale (VAS) 3. Requiring anti-inflammatory therapy assignment 4. NSAID-gastropathy or dyspepsia development from NSAID therapy in anamnesis 5. Informed patient consent to administer the preparation 6. Compliance with the listed research protocol

Exclusion criteria

Exclusion criteria: 1. Ulcer presence during upper gastrointestinal (GI) endoscopy and more than 5 stomach mucosa and/or duodenum erosions, and/or erosive oesophagitis 2. High risk of cardiological complications, arterial hypertension, cardiac insufficiency greater than II degree, myocardial infarction or apoplectic attack in anamnesis during the previous 3 years, chronic kidney disease, liver insufficiency, bronchial asthma, subcompensated or decompensated diabetes mellitus, oncological diseases 3. NSAID administration, aspirin in anti-aggregant doses, glucocorticosteroids 4. Pregnancy

Design outcomes

Primary

MeasureTime frame
Upper GI lesions (erosion, ulcer) were assessed on the 28 day of treatment with upper GI endoscopy

Secondary

MeasureTime frame
Gastritis

Countries

Russian Federation

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026