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Postoperative Pain clinical trials

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NCT ID: NCT01701921 Completed - Postoperative Pain Clinical Trials

The Effects of Pregabalin on Postoperative Pain After Cardiac Surgery

Start date: July 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether pregabalin is effective in the treatment of acute postoperative pain after cardiac surgery if administered before the surgery.

NCT ID: NCT01699919 Completed - Postoperative Pain Clinical Trials

A Study to Assess Analgesic Efficacy of Intravenous Lignocaine

Start date: April 2011
Phase: Phase 4
Study type: Interventional

The primary objectives of this study are to analyse the effect of perioperative systemic infusion of lignocaine on postoperative pain, postoperative nausea and vomiting and perioperative levels of inflammatory mediators in patients undergoing elective open abdominal surgeries. The secondary parameters which will be observed during the study are the time to passage of flatus and stools postoperatively.

NCT ID: NCT01693588 Completed - Pain Clinical Trials

Study of a Multimodality Pain Management Protocol on Postoperative Neurosurgical Pain

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

High levels of postoperative pain are associated with an increased risk of lung and heart complications, are the most common reason for delayed discharge or for unexpected hospital admission after ambulatory surgery, and are responsible for prolonged recovery after inpatient surgery. Furthermore both neuropathic pain and post surgical pain inhibit weight gain and may have an impact on the patient's nutrition post operatively. The purpose of this study is to evaluate the effectiveness of a multimodality pain management protocol on postoperative neurosurgical pain.

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: 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: 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: NCT01666379 Completed - Postoperative Pain Clinical Trials

Pain Management After Forefoot Surgery

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study was to compare the efficacy of transdermal fentanyl to placebo both administered together with peroral nonsteroidal antiinflammatory drug (NSAID) and paracetamol in treatment of postoperative pain after hallux valgus or hallux rigidus surgery.

NCT ID: NCT01662401 Completed - Postoperative Pain Clinical Trials

Postoperative Pain Control in Children Undergoing Laparoscopic Appendectomy: Peripheral Nerve Block Versus Local Anesthetic

Start date: May 2008
Phase: Phase 2
Study type: Interventional

After undergoing a laparoscopic appendectomy, a child may experience some degree of pain in the postoperative period. As a routine part of the procedure, surgeons inject local anesthetic where the laparoscopic ports are placed. This provides some pain relief, but most children will still require additional pain medications after surgery. The purpose of the study is to see if a combination of peripheral nerve blocks (rectus sheath and ilioinguinal nerve) will give better pain relief, decreasing pain medication requirements and increasing comfort during the postoperative period.

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.