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Postoperative Pain clinical trials

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NCT ID: NCT01919606 Terminated - Postoperative Pain Clinical Trials

EXPAREL Administered Into the TAP for Analgesia in Subjects Undergoing Open Total Abdominal Hysterectomy

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

The primary objective of this study is to determine the optimal of two different volumes of EXPAREL 266 mg when administered via infiltration into the transversus abdominis plane (TAP) for prolonged postoperative analgesia in subjects undergoing open total abdominal hysterectomy.

NCT ID: NCT01909765 Not yet recruiting - Postoperative Pain Clinical Trials

Two Different Surgical Techniques on Postoperative Circumcision Pain

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

To compare the effect of two different surgical techniques, the dorsal slit and double incision technique, on postoperative pain.

NCT ID: NCT01898052 Completed - Postoperative Pain Clinical Trials

The Efficacy of Periarticular Single Drug Compared With Multimodal Drug Injection in Controlling Pain After TKA

TKA
Start date: October 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the periarticular multimodal drug injection has more efficacy for controlling pain after TKA than single anaesthetic drug injection.

NCT ID: NCT01881776 Completed - Postoperative Pain Clinical Trials

Continuous Interscalene Block Results in Superior Recovery Throughout the First Postoperative Week

Start date: August 2011
Phase: Phase 0
Study type: Interventional

The investigators undertook this prospective, randomized trial to compare the recovery profile throughout the first postoperative week in patients receiving continuous (CISB) interscalene brachial plexus block, single injection (SISB), or general anesthesia (GA) for arthroscopic rotator cuff repair surgery. Specifically, the effects of the three anesthetic techniques when used intraoperatively as a sole anesthesia modality were studied on postoperative pain, time-to-first pain, analgesic consumption, fast-tracked PACU bypass rate, length of PACU stay, time-to-discharge home, sleep duration, and related adverse effects. The investigators hypothesized that CISB results in a superior postoperative recovery profile as compared to SISB or GA alone.

NCT ID: NCT01870973 Completed - Postoperative Pain Clinical Trials

Effect of Root Canal Treatment (Versus no Treatment) for Patients With Tooth Infections and Toothaches

Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate patients with emergency pain and a sore (infected) tooth to determine if immediate root canal therapy is better at reducing pain, when compared to initial treatment with antibiotic and pain medication followed by root canal therapy. Each participant will be randomly assigned a number, which will determine if they will receive initial endodontic treatment that day or at a later date. Each participant will receive an anesthetic injection, pain medication and a prescription for an antibiotic. They will be asked to keep a diary to record their pain level after the injection and their pain levels and the amount and type of pain medication taken each day for the next 5 days. Participants who did not receive root canal therapy at the initial appointment will receive it after the 5 day postoperative period. The pain levels and medication use will be compared between the treatment and nontreatment groups.

NCT ID: NCT01868633 Completed - Postoperative Pain Clinical Trials

Dexamethasone for Post Cesarean Delivery Analgesia

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

The purpose of this study is to assess the effectiveness intravenous (IV) dexamethasone when used as part of a multimodal regimen to manage post cesarean delivery pain. We hypothesize that a single dose of IV dexamethasone administered, as part of a multimodal analgesia after spinal anesthesia will significantly reduce post cesarean delivery opioid consumption and pain

NCT ID: NCT01859585 Completed - Postoperative Pain Clinical Trials

Efficacy Parecoxib and Ketorolac as Preemptive Analgesia in Spine Fusion

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

The purpose of this study is to evaluate the efficacy of Parecoxib and Ketorolac as a preemptive analgesia in patients undergoing lumbar spinal fusion.

NCT ID: NCT01837394 Completed - Postoperative Pain Clinical Trials

Ultrasound-guided Blocks for Ambulatory Knee Arthroscopy

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

In this study, we wish to investigate the effect of ultrasound (US) -guided block of the saphenous nerve (SN) and the posterior branch of the obturator nerve (ONP) on postoperative pain and the use of opioids (morphine-like pain medicine) in the first 24 hours following ambulatory knee arthroscopy. We wish to investigate the analgesic effect of these two blocks compared to placebo (injection of local anesthetic with known pain blocking properties compared with injection of a saline solution), when used as a supplement to conventional oral analgesics. We hypothesize that patients receiving the active treatment may experience less pain during the first 24 hours after their operation than patients receiving the placebo treatment, and possibly require less opioid analgesics, experience less opioid related side effects and have a higher function level in this period than patients receiving the placebo treatment.

NCT ID: NCT01835106 Withdrawn - Postoperative Pain Clinical Trials

Efficacy of an Epidural Versus a Fascia Iliaca Compartment Catheter After Hip Surgery

Start date: April 2013
Phase: N/A
Study type: Interventional

The investigators are investigating two ways of treating pain after hip surgery. One way is though a thin tube (called a catheter), and it is placed into the back so that pain-numbing drugs can reach the nerves near the backbone. This is called an "epidural" catheter. Another way is to place the catheter close to the hip, where the surgery is done, so that the pain-numbing drugs can reach some of the nerves more locally. This is called a "fascia iliaca compartment" catheter. The investigators do not know which way is best to treat pain, or has fewer side effects, or allows a patient to leave hospital faster. Usually, patients would receive only one type of catheter for pain relief. To do this comparison, the investigators would place both catheter types, so that patients help us tell which one works better.

NCT ID: NCT01816386 Completed - Postoperative Pain Clinical Trials

Acupuncture Trial for Post Anaesthetic Recovery and Postoperative Pain

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

In the present study, the investigators want to evaluate if press needle acupuncture applied prior to surgery may contribute to the anaesthesiologic outcome. Acupuncture might improve fast-track anaesthesia in the PACU after general surgery.