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Pain, Postoperative clinical trials

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NCT ID: NCT01636700 Withdrawn - Postoperative Pain Clinical Trials

Tramadol Infiltration for Tonsillectomy

Start date: October 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the analgesic effect and IL-6 after tramadol infiltration or intravenous for tonsillectomy.

NCT ID: NCT01622322 Withdrawn - Post Operative Pain Clinical Trials

Nitrous Oxide On Acute Postoperative Pain and Opioid Consumption and Chronic Pain After Inguinal Hernia Repair Surgery

Start date: May 2012
Phase: N/A
Study type: Interventional

To compare postoperative pain, opioid consumption and chronic pain in patients undergoing to hernia repair surgery after receiving nitrous oxide or oxygen during the general anesthesia.

NCT ID: NCT01591980 Withdrawn - Headache Clinical Trials

Effects of Perioperative Pregabalin for Post-Craniotomy Pain

Start date: August 2013
Phase: Phase 4
Study type: Interventional

Objective: To compare the incidence of chronic pain at 3 months among adults undergoing craniotomy between those received two different doses of pregabalin and those receiving placebo.

NCT ID: NCT01511627 Withdrawn - Hysterectomy Clinical Trials

Randomized Controlled Trial Comparing Postoperative Pain Following TAH With GA vs. Combined GA + SAB

Start date: January 2012
Phase: N/A
Study type: Interventional

The investigators hypothesize that a spinal anesthetic administered prior to the induction of general anesthesia will result in reduced need for pain medication and reduced postoperative pain, as well as reduced hospital stay following a total abdominal hysterectomy.

NCT ID: NCT01494259 Withdrawn - Pain Clinical Trials

Bupivacaine Pain Pumps to Decrease Mastectomy Post-Operative Pain

Start date: January 2016
Phase: Phase 4
Study type: Interventional

This double-blind, randomized, controlled clinical trial comparing patient-reported pain and pain medication/narcotic use between patients randomized to treatment (bupivacaine) or placebo (saline) delivered via pain pump to the mastectomy site. Candidates will have chosen to have a mastectomy on one side immediately followed with tissue expander placement breast reconstruction. Patients will be randomized 1:1 to bupivacaine- (treatment) or saline-(placebo) filled percutaneously-placed pain pumps; neither the participants nor the study staff will know participants' treatment. Data on patient-perceived pain and pain medication use will be collected before surgery, during surgery, and after surgery on Days 1, 2, 3, 7, and 90, and at Years 2 and 4 by phone. The investigators hypothesize that patients randomized to the treatment (bupivacaine) group will have significantly lower pain scores and use less pain medicine than patients who receive placebo during the first 90 days following their surgery. The Year 2 and Year 4 follow-ups are included as tertiary endpoints to capture differences in chronic pain, and patients will be asked to complete the same questionnaires as at the Day 90 follow up.

NCT ID: NCT01374828 Withdrawn - Pain, Postoperative Clinical Trials

Ketolorac Versus Saline at Laparoscopic Incision Sites

Start date: January 2012
Phase: Phase 4
Study type: Interventional

Pain control following surgery is a critical aspect of patient care. Pain at incision sites in laparoscopic surgery contributes to overall pain felt by a patient. There is no definitive proof that the typical medications (such as lidocaine) injected at incision sites during surgery improve pain control. This study looks at a different type of medication (ketorolac - an NSAID) to better control pain at laparoscopic incision sites.

NCT ID: NCT01324544 Withdrawn - Clinical trials for Other Acute Postoperative Pain

Pharmacokinetics, Safety, and Efficacy of Intravenous Dosing of Buprenorphine in Pediatric Patients Who Require Opioid Analgesia for Acute Moderate to Severe Pain

Start date: November 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to characterize the safety, pharmacokinetics (PK), and efficacy of intravenous (IV) buprenorphine in pediatric patients.

NCT ID: NCT01231191 Withdrawn - Postoperative Pain Clinical Trials

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of the Relationship Between Intraoperative Intravenous Acetaminophen and Postoperative Opioid Avoidance for Ambulatory Surgical Procedures

Cadence
Start date: n/a
Phase: Phase 4
Study type: Interventional

This is a research study to determine if giving acetaminophen intravenously in hte operating room will decrease the number of patients who require additional pain medicine, such as morphine, after surgery in the recovery room.

NCT ID: NCT01190722 Withdrawn - Postoperative Pain Clinical Trials

A Study Comparing Etoricoxib and Diclofenac Sodium in Post Hallux Valgus Surgery Pain

Start date: November 10, 2010
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that cyclooxygenas-II-selective inhibitors (Coxibs) provide a better patients assessed overall satisfaction when used for pain management after elective hallux valgus surgery as compared to traditional Non-steroidal anti-inflammatory drugs (NSAIDs).

NCT ID: NCT01125059 Withdrawn - Postoperative Pain Clinical Trials

Methadone Versus Placebo in Spine Fusion

Start date: May 2010
Phase: N/A
Study type: Interventional

What is the influence of methadone on postoperative analgesia after lumbar interbody fusion in opioid naïve patients or patients who are taking less than equivalent of 15 mg IV morphine each day? What is the incidence of opioid related postoperative side effects after the administration of methadone in the operating room?