Post-Operative Pain Management With NSAIDS

Completed

Conditions studied: Urogynecologic Surgery

In brief

Specific Aim 1: To identify differences in pain perception and satisfaction with pain control in women undergoing urogynecologic surgery receiving nonsteroidal anti-inflammatory (NSAIDS) postoperatively by oral ibuprofen, intravenous ibuprofen, or intravenous ketorolac. Specific Aim 2: To compare the differences in narcotic usage and medication side effects.

Key facts

Study ID

NCT01971372

Run by

University of Oklahoma

People needed

120

Starts

2013-09-01

Expected to finish

2015-11-01

Last updated by the study team

2016-06-09

Who can join

Age: 18 and older, up to 99. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female gender
• Available for reliable follow up
• Able to complete study assessment
• Scheduled for surgery by FPMRS surgeon

You may not qualify if…

• Age <18 years
• Known renal impairment
• Congestive heart failure
• Dementia or inability to follow instructions
• Allergy to NSAIDS
• Allergy to hydromorphone
• History of gastrointestinal bleeding or ulceration
• Inflammatory bowel disease

Where it is running

• University of Oklahoma Health Sciences Center — Oklahoma City, Oklahoma, United States

Full record on ClinicalTrials.gov

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