A study on the effect of information on the use of analgesics in patients after weight loss surgery.

• Conditions: use of NSAIDSbariatrische chirurgie; gebruik van NSAID's; bariatric surgery

• Registration Number: NL-OMON25083
• Lead Sponsor: Medisch Centrum Leeuwarden (MCL), Leeuwarden, The NetherlandsMedisch Centrum Leeuwarden (MCL), H. Dunantweg 2, 8934 AD Leeuwarden

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 240

Inclusion Criteria

1. Patients who underwent bariatric surgery in Medisch Centrum Leeuwarden (MCL) in the period March to November 2011;

2. Patients who signed and turned in a written informed consent.

Exclusion Criteria

Patients with no medication record at any moment of the study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The percentage of users of NSAIDS in the period 6 months before the intervention and in the period 3 to 9 months after the intervention in comparison with the control group. The use is determined by collecting dispensing data from pharmacies 6 months before the intervention and 9 months after the intervention. The use of NSAIDS is to be considered as stopped if there is no use of an NSAID any more in the period 3 to 9 months after the intervention.