Clinical Trials Logo

Post-operative Pain clinical trials

View clinical trials related to Post-operative Pain.

Filter by:

NCT ID: NCT00849719 Not yet recruiting - Post Operative Pain Clinical Trials

Effects of a Combination of IV-PCA With Continuous IV Infusion of MO, Versus IV-PCA MO on Postoperative Pain

Start date: April 2009
Phase: N/A
Study type: Interventional

After major surgery, such as abdominal or thoracic surgery, the majority of patients experience moderate to severe pain that may not be optimally controlled. Inadequate pain relief may lead to complications that can hinder rehabilitation and slow recovery. Morphine (MO) is the most commonly used opioid for the treatment of post-surgical pain (14). The preferred method of administration nowadays is intravenous patient-controlled analgesia (PCA). In contrast, Continuous infusion of intravenous morphine (CIVM) is seldom used in Post-Anesthesia Care Units (PACUs) for acute postoperative pain, due to concerns of cardio-respiratory deterioration, even though different studies have found this technique of administration effective and safe (in terms of opioid-related symptoms.As part of our efforts to improve postoperative pain management in the Tel Aviv Sourasky Medical Center's PACU, we wish to determine if combining CIVM with IV PCA will be superior over IV PCA only for the treatment of postoperative pain following major abdominal or thoracic surgery.Our hypothesis is that the continuous infusion, even if given at a relatively low dose, would enable the build-up of pharmacologically effective MO blood level, thus providing an overall better control of pain.

NCT ID: NCT00847093 Completed - Post-Operative Pain Clinical Trials

LMX-4 for Postoperative Pain Management in Infants and Children Undergoing Penoplasty Surgery

LMX-4
Start date: September 2008
Phase: Phase 4
Study type: Interventional

After surgery on his penis, your child will probably have some pain. The investigators will give you a prescription for acetaminophen (Tylenol) with codeine, given by mouth (orally), for pain. In this study, the investigators want to see if a local anesthetic cream applied to the base of the shaft of the penis can reduce the need for oral medicine .

NCT ID: NCT00830089 Completed - Clinical trials for Postoperative Complications

Trial of a Transversus Abdominis Plane (TAP) Block in Laparoscopic Colorectal Surgery

Start date: September 2009
Phase: N/A
Study type: Interventional

Keyhole surgery for bowel disease has brought great benefits, enabling patients to recover quicker from surgery and so return to normal activities. Although keyhole surgery reduces pain following abdominal surgery, it still causes enough pain to require strong pain killing medications such as morphine-like drugs which, although good pain killers, can have a detrimental effect on the recovery of bowel function, leading to feelings of nausea and vomiting and ultimately delaying recovery. These side-effects can reduce the potential benefits from keyhole surgery and our "fast-track" recovery programmes. The aim of this project is to assess the effectiveness of a new method of pain control after keyhole bowel surgery. The study involves the injection of local anaesthetic into the abdominal muscles once the patient is anaesthetised. Although use of local anaesthetic is common practice, we are looking at a new technique of injecting it called a transversus abdominis plane (or TAP) block. This technique will attempt to block the pain nerves to the abdomen prior to the operation beginning. We plan to investigate whether this new technique will reduce the amount of pain following keyhole bowel surgery. If successful, it might be used to further enhance people's recovery from bowel surgery.

NCT ID: NCT00795223 Completed - Post Operative Pain Clinical Trials

Comparative Pain Control Between 0.2 or 0.3 Spinal Morphine and 0.25 or 0.5 % Bupivacaine for FNB After TKA

Start date: October 2008
Phase: Phase 4
Study type: Interventional

Comparative efficacy of 24 and 48 hours post operative pain control in single total knee replacement between intrathecal bupivacaine with 0.2 or 0.3 mg morphine together with 0.25 or 0.5 % bupivacaine for single femoral nerve block

NCT ID: NCT00791804 Completed - Pain Clinical Trials

Phase II Study of Inhaled AeroLEF for Analgesia After ACL Knee Surgery

Pain
Start date: February 2004
Phase: Phase 2
Study type: Interventional

To evaluate the safety and efficacy of self-titration to effective analgesia with inhaled AeroLEF in patients with moderate/severe acute pain in the post-surgical setting.

NCT ID: NCT00743730 Completed - Post Operative Pain Clinical Trials

Parent Nurse Controlled Analgesic in Pediatric Patients With Developmental Delay

PNCA
Start date: June 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to compare, the safety, efficacy and level of parent and nurse satisfaction with three methods of opioid administration post-operatively in children (4-18 years of age) with developmental delay.

NCT ID: NCT00707057 Completed - Pain Clinical Trials

Ibuprofen Extended-Release Dental Pain Study

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of multiple doses of Ibuprofen 600 mg Extended-Release Tablets in a study of dental pain following extraction of third molar teeth.

NCT ID: NCT00695240 Recruiting - Clinical trials for Pelvic Organ Prolapse

Post-Operative Pain Control Using Direct Continuous Bupivacaine Infusion After Pelvic Organ Prolapse Repair

Start date: April 2007
Phase: Phase 2/Phase 3
Study type: Interventional

This prospective randomized controlled study will determine the efficacy of continuous local anesthesia at decreasing pain scores compared to patient controlled analgesia for pelvic organ prolapse procedures including posterior colporrhaphy and sacrospinous ligament fixation.

NCT ID: NCT00672100 Completed - Post-operative Pain Clinical Trials

Initial Local Anesthetic Dose With Continuous Interscalene Analgesia

Start date: January 2009
Phase: N/A
Study type: Interventional

Objective: To determine a minimally effective initial local anesthetic bolus required to provide satisfactory analgesia using continuous brachial plexus infusion following arthroscopic shoulder surgery using a double-blind, randomized, study comparing 3 initial doses.

NCT ID: NCT00643032 Not yet recruiting - Post-Operative Pain Clinical Trials

Preoperative Anxiety and Postoperative Pain in Children

Start date: March 2008
Phase: Phase 4
Study type: Interventional

We wish to study which method of local injection of analgesic (before or during surgery) is the more effective method to reduce post-operative pain in children. In addition, we wish to study which pre-operative educational intervention is more effective in reducing anxiety in children and their family.