A Comparison of the Effectiveness and Safety of ULTRACET® (Tramadol Hydrochloride/Acetaminophen) Versus ULTRAM® (Tramadol Hydrochloride) Versus Placebo in Patients With Pain After Oral Surgery
Surgery, Oral, Pain, Postoperative
About this trial
This is an interventional treatment trial for Surgery, Oral focused on measuring Oral Surgery, Analgesics, Postoperative Pain, dental
Eligibility Criteria
Inclusion Criteria: Surgical procedure involving removal of >= 2 impacted third molars with bone removal required for at least 2 of the 3 impacted third molars At least moderate pain within 5 hours after oral surgery procedure Sufficiently alert to follow directions, communicate with study personnel and perform study procedures If female, using an acceptable method of birth control and has a negative urine pregnancy test Exclusion Criteria: Previously treated patients who have discontinued treatment due to an adverse event Patients who have had inadequate pain relief from tramadol HCl/acetaminophen or tramadol Patients who have used pain medication (other than anesthesia) within 24 hours of receiving study medication, any long-acting over-the-counter pain medications within 3 days, or any pain medication after finishing oral surgery Patients with known problems with taking opioid medications or acetaminophen Patients with a history of abusing drugs or alcohol Patients with an uncontrolled medical condition