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Upper GI Symptoms In Patients Receiving Acetylsalicylic Acid/NSAIDs - NSAIDs Wave 2 (NSAIDS II)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Upper-GI Symptoms

Study type

Observational

Funder types

Industry

Identifiers

NCT00691743
NIS-GGR-DUM-2008/1

Details and patient eligibility

About

The current epidemiological study will be undertaken in GP's and specialized private doctors. In total, 85 general practitioners, orthopedics, rheumatologists and cardiologist will take part in the study. Data will be collected for 850 patients who visit their physician for medical conditions that require the use of acetylsalicylic acid and/or NSAIDS. The first 10 consecutive patients who visit their GP/orthopedic/rheumatologist/cardiologists and are currently receiving acetylsalicylic acid and/or NSAIDS will be included in the study.

Enrollment

850 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Acetylsalicylic acid/NSAIDS intake for at least 5 days of a week during the past month before the patient's visit to the clinician

Exclusion criteria

  • Patients who are not willing to sign of the Informed Consent Form

Trial design

850 participants in 1 patient group

1
Description:
Primary care

Trial contacts and locations

27

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Data sourced from clinicaltrials.gov

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