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Postoperative Pain clinical trials

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NCT ID: NCT03372304 Completed - Postoperative Pain Clinical Trials

Catheter-based Peripheral Regional Anesthesia After Orthopedic Surgery to the Foot or Ankle

API-FOOT
Start date: November 29, 2017
Phase: Phase 4
Study type: Interventional

BACKGROUND Orthopedic surgery can be severely painful, and peripheral regional anesthesia is highly recommended as part of the perioperative pain treatment. Whether catheter-based techniques are better than single injection techniques are debatable. Furthermore, in catheter-based techniques, whether a low-dose automated, periodic infusion can produce similar analgesic effectiveness compared to a conventional, high dose, continuous infusion has never been explored. AIM Comparison of the analgesic effectiveness of a low-dose automated, periodic infusion, a conventional continuous infusion and patient-controlled boluses only in catheter-based nerve blocks for patients undergoing orthopedic surgery to the foot or ankle.

NCT ID: NCT03372265 Completed - Postoperative Pain Clinical Trials

Catheter-based Peripheral Regional Anesthesia After Total Knee Arthroplasty

API-KNEE
Start date: December 6, 2017
Phase: Phase 4
Study type: Interventional

BACKGROUND Total knee arthroplasty can be severely painful, and peripheral regional anesthesia is highly recommended as part of the perioperative pain treatment. Whether catheter-based techniques are better than single injection techniques are debatable. Furthermore, in catheter-based techniques, whether a low-dose automated, periodic infusion can produce similar analgesic effectiveness compared to a conventional, high dose, continuous infusion has never been explored. AIM Comparison of the analgesic effectiveness of a low-dose automated, periodic infusion, a conventional continuous infusion and patient-controlled boluses only in catheter-based adductor canal blocks for patients undergoing total knee arthrplasty.

NCT ID: NCT03369392 Completed - Postoperative Pain Clinical Trials

PANDA-Regional Feasibility Study of a Smartphone Pain Management Application

Start date: December 11, 2017
Phase: N/A
Study type: Interventional

Despite the numerous benefits of peripheral nerve blocks (PNBs) over general anesthesia (GA) in a variety of surgical procedures, PNBs can be associated with increased post-operative pain if pain medications are not taken correctly (titrated). Unfortunately, this is a common occurrence as patients often have difficulty titrating medications in the absence of direct medical care. PANDA, a smartphone-based postoperative pain management tool, is designed to address this issue by helping patients manage their pain medications. The purpose of this study is to demonstrate the feasibility of this application in patients who are discharged after receiving PNBs. The goal is to identify areas of improvement for the application itself. It is hypothesize that PANDA will be successful in supporting patients' postoperative pain management.

NCT ID: NCT03354572 Completed - Postoperative Pain Clinical Trials

Pilot Study: Postoperative Pain Reduction by Pre Emptive N-Acetylcysteine

Start date: October 20, 2017
Phase: Phase 4
Study type: Interventional

Despite current available analgesic drugs, post-surgical pain management remains challenging. A potential new target for analgesic drugs are group-II metabotropic glutamate receptors subtypes (mGlu2 and mGlu3 receptors), since growing evidence from animal models show that activation of these receptors produce s analgesic effects in inflammatory and in neuropathic pain states. . N-Acetylcysteine (NAC) is a safe agent and with little to no side effects. NAC can induce analgesia by activating the glutamate:cystein antiporter, causing endogenous activation of the mGlu 2/3 receptors. However, this has only been investigated once in the peri-operative setting, were it showed preliminary promising result of reduction in opiate necessity. In healthy subjects there was a significant reduction in pain ratings to laser stimuli and amplitudes of laser evoked potentials after NAC. Based on these promising results, we hypothesize that pre emptive intravenous NAC can reduce postoperative pain and thereby cause less necessity for escape analgesics like opiates.

NCT ID: NCT03350334 Completed - Postoperative Pain Clinical Trials

Perioperative Duloxetine for Pain Management After Laparoscopic Hysterectomy

Start date: December 4, 2017
Phase: N/A
Study type: Interventional

The aim of the investigators of the study is to evaluate the effect of peri-operative duloxetine on post-operative recovery in patients undergoing laparoscopic hysterectomy.

NCT ID: NCT03343509 Completed - Postoperative Pain Clinical Trials

Topical Versus Oral Metronidazole Following Excisional Haemorrhoidectomy

Start date: March 11, 2019
Phase: Phase 4
Study type: Interventional

This study aims to determine if topical metronidazole reduces pain more than oral metronidazole following excisional haemorrhoidectomy. The trial will be a multi-centered, patient and investigator blinded superiority trial with two parallel groups and a primary outcome of pain scores during 14 days after surgery. Group A will receive oral metronidazole and placebo cream. Group B will receive placebo tablets and topical metronidazole cream.

NCT ID: NCT03332316 Completed - Postoperative Pain Clinical Trials

Effect of Perineural Dexamethasone on the Duration of Popliteal Nerve Block for Anesthesia After Ankle Surgery

Start date: November 2, 2017
Phase: Phase 4
Study type: Interventional

Effect of perineural dexamethasone on the duration of popliteal nerve block after ankle/foot surgery

NCT ID: NCT03328988 Completed - Postoperative Pain Clinical Trials

QLB and Radical Cystectomy, Postoperative Pain

BladderQLB
Start date: April 27, 2017
Phase: N/A
Study type: Interventional

There are ca 1000 new cases of bladder cancer in Finland/year. The curative therapy for high risk bladder cancer is radical cystectomy. The golden standard is still an open surgery despite development of laparoscopic techniques. Epidural analgesia is considered as most effective for the treatment of postoperative pain. However, there is a need for other effective options, because epidural analgesia has some contraindications and risks for serious complications. Recently quadratus lumborum block has gained popularity in the treatment of postoperative pain after various surgeries in the area from hip to mamilla. It is more beneficial than other peripheral blocks, since it covers also the visceral nerves. Contrary to the need of epidural catether a single shot QLB has reported to last up to 48 hours. Inadequately treated acute postoperative pain is considered as one of the main risk factors for persistent postoperative pain. 44 patients aging 18-85 will be recruited based on a power calculation. The primary outcome measure is the acute postoperative need for rescue analgesics. Secondary outcomes are acute pain (NRS scale), nausea, vomiting, mobilisation and longterm outcomes such as quality of life and persistent pain.

NCT ID: NCT03328299 Completed - Postoperative Pain Clinical Trials

Pharmacokinetics and Dynamics of Dexmedetomidine as Adjuvant in TAP Block

Start date: November 11, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

TAP-block has been shown to be a safe and effective postoperative analgesia method in a variety of general. Dexmedetomidine is a selective α2 agonist with 8 times more affinity for α2 adrenergic receptors compared to clonidine and possesses all the properties of α2 agonist without respiratory depression. Dexmedetomidine has been focus of interest for its broad spectrum (sedative, analgesic and anesthetic sparing) properties, making it a useful and safe adjunct in many clinical applications.

NCT ID: NCT03319277 Completed - Postoperative Pain Clinical Trials

A Randomized-controlled Trial of Post-operative Opiate Quantities After Urogynecologic Surgery

Start date: October 13, 2017
Phase: N/A
Study type: Interventional

This is a randomized controlled trial to determine the effect of decreased post-operative prescriptions of opiate medications after urogynecologic surgery.