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Post-Operative Pain Management With NSAIDS

NCT01971372 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2016-06-09

No results posted yet for this study

Summary

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.

Conditions

  • Urogynecologic Surgery

Sponsors & Collaborators

  • University of Oklahoma

    lead OTHER

Principal Investigators

  • Mikio Nihira, MD · University of Oklahoma

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-11-30
Completion
2015-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01971372 on ClinicalTrials.gov