Columbia University Medical Center
New York, 10032, United States
NCT Number: NCT00845754
The purpose of this study is to determine if ketorolac, given after abdominal myomectomy, will decrease the frequency of post-oerative fevers as well as improve post-operative pain management.
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Notify Me18 year and older
Female
Interventional
Not applicable
New York, 10032, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
15mg IV every6 hours for 4doses
Other names: Toradol
15mg IV every 6hrs for 4 doses
Time frame: Inital 24hrs post-operative
Time frame: Initial 24hrs post-operative
Ascher-Walsh, Charles, M.D.
Indiv
Effects of Ketorolac on Post-Operative Febrile Morbidity and Pain Management in Abdominal Myomectomy Patients
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