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Pain, Postoperative clinical trials

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NCT ID: NCT01691937 Completed - Clinical trials for Right Lobe Hepatectomy

Continuous Paravertebral Block on Postoperative Pain After Hepatectomy

Start date: September 2012
Phase: Phase 2
Study type: Interventional

Patients often experience moderate to severe postoperative pain, especially during the first hours after hepatectomy. Systemic opioids given with patient-controlled analgesia has be used after hepatectomy in many medical center(Aubrun, Monsel et al. 2001; Aubrun, Salvi et al. 2005), but the analgesic effect can be limited and undesirable side effects may occur. A case report described that right thoracic paravertebral block reduced pain and analgesic requirements after right lobe hepatectomy(Ho, Karmakar et al. 2004). Compared with epidural analgesia, thoracic paravertebral block probably carries a much lower risk of spinal haematoma in the presence of moderate haemostatic deficiencies (Richardson and Lonnqvist 1998; Karmakar 2001). We therefore designed a prospective, randomized, subject and assessor blinded, parallel-group, placebo controlled study to test the hypothesis that continuous right thoracic paravertebral analgesia decreases opioid consumption during the first 24 h after right lobe hepatectomy in patients receiving i.v. patient-controlled analgesia (PCA) with sufentanil.

NCT ID: NCT01688596 Completed - Pain, Postoperative Clinical Trials

Injection of Local Anesthetic to Trocar Insertion Sites After Laparoscopy

Start date: September 2012
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to assess if injection of local anesthetic to the laparoscopic trocar sites after a hysterectomy will make a difference in a patient's pain after surgery.

NCT ID: NCT01686802 Completed - Post-operative Pain Clinical Trials

Post-operative Oral Morphine Versus Ibuprofen

Start date: September 2012
Phase: Phase 2
Study type: Interventional

Children 5-17 years of age who have undergo orthopedic day surgical procedures for definitive management of fractures, tendon release, etc. will be randomized to receive either ibuprofen or oral morphine as needed for pain relief for 48 hours post-operatively at home. Pain will be assessed using the self-report Faces pain scale revised (FPS-R). We hypothesize that oral morphine will result in significantly lower pain scores on the Faces Pain Scale Revised (FPS-R) compared to ibuprofen. It is hoped that the results of this trial will create a new option for post-operative pain management in children.

NCT ID: NCT01685593 Completed - Postoperative Pain Clinical Trials

Abdominal Binder Study to Decrease Postoperative Pain

Start date: January 2001
Phase: N/A
Study type: Interventional

We conducted a controlled randomized trial examining the ability of the Mott abdominal Compression Binder to decrease postoperative pain in gynecologic abdominal laparotomy patients

NCT ID: NCT01683071 Completed - Postoperative Pain Clinical Trials

Femoral Nerve Block With Liposome Bupivacaine for Postsurgical Analgesia Following Total Knee Arthroplasty

Start date: September 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objectives of Part 1 are to (1) evaluate three dose levels of liposome bupivacaine versus placebo with respect to the magnitude and duration of the analgesic effect achieved following single dose injection femoral nerve block with liposome bupivacaine, and (2) select a single therapeutic dose of liposome bupivacaine from the three dose levels to be tested in Part 2. Part 2: The primary objective of Part 2 is to compare the magnitude and duration of the analgesic effect of single injection femoral nerve block of a single dose level of liposome bupivacaine (selected from Part 1) with placebo (preservative-free normal saline).

NCT ID: NCT01681966 Completed - Post Operative Pain Clinical Trials

A Single-dose Open-Label Study to Assess the Safety and Preliminary Efficacy of PRF 110 in Open Herniorrhaphy Surgery

Start date: September 2012
Phase: Phase 2
Study type: Interventional

LNP is new extended release (ER) oily solution formulation of ropivacaine that is intended for local infiltration into surgical wounds. The purpose of this study is to determine the ease of usage and administration of LNP in the surgical setting, to follow the Pharmacokinetic (PK) profile of LNP over 72 hours and evaluate the duration of analgesia witnessed in the surgical setting.

NCT ID: NCT01680549 Completed - Postoperative Pain Clinical Trials

Pain Control With Total Knee Replacement

L12-078
Start date: September 2012
Phase: Phase 4
Study type: Interventional

The purpose of this project is to study the effects of gabapentin on pain control in the perioperative and post-operative period of total knee arthroplasty.

NCT ID: NCT01677143 Completed - Pain, Postoperative Clinical Trials

Pre-emptive Local Anaesthesia in Gynecological Laparoscopy

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

Pre-emptive local anaesthetics are widely used in laparoscopic surgery, but there is no really consistent evidence that it is useful. Studies in the literature have shown contradicting results. At our hospital we are currently using pre-emptive local anaesthetics in the trocar areas, but as the literature does not give a clear and clinically relevant answer, we need to find out more. This study aims to see if pre-emptive local anaesthetics are useful in the setting of our day-case, laparoscopic surgery.

NCT ID: NCT01675635 Completed - Postoperative Pain Clinical Trials

OxyNorm Capsules in Post-Operative Pain Study

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

The efficacy and safety of oxycodone capsules compared with morphine tablets in hospitalized patients with moderate to severe pain following surgery.

NCT ID: NCT01667445 Completed - Osteoarthritis Clinical Trials

Evaluation of the Use of Spinal Epimorph in Total Knee Arthroplasty

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

The purpose of this study is to determine the contribution of spinal epimorph to patient's perioperative pain management in Total Knee Arthroplasty (TKA). This study is designed to determine whether spinal epimorph and its associated complications is a necessary addition to provide adequate analgesia given the multimodal approach to pain management. It is hypothesized that perioperative local infiltration with a cocktail of local and systemic analgesics will provide equal analgesia to patients who are given both local infiltration and spinal epimorph perioperatively.