Clinical Trials Logo

Acute, Post-operative Pain clinical trials

View clinical trials related to Acute, Post-operative Pain.

Filter by:
  • None
  • Page 1

NCT ID: NCT06075498 Completed - Prostate Cancer Clinical Trials

Comparison of Analgesia Efficacy of Transversus Abdominis Plane Block and Posterior Approach Quadratus Lumborum Block

Start date: February 5, 2022
Phase: N/A
Study type: Interventional

Prostate cancer is the second most common cancer and the fifth in cancer-related deaths. Open radical retropubic prostatectomy is the most common surgical treatment for localized prostate cancer. Open radical retropubic prostatectomy is associated with moderate pain. Severe pain in the postoperative period affects the length of hospital stay and morbidity. Multimodal analgesia applications for the management of postoperative pain are the main component of post-surgical recovery. Different analgesia modalities, including systemic opioid use and neuraxial analgesia, have been used for pain control after retropubic radical prostatectomy. Side effects of systemic and intrathecal opioids limit the potential benefits of these agents. Transversus abdominis plane block and quadratus lumborum block are blocks that can be used for postoperative analgesia in the abdominal and pelvic regions. There is no study in the literature comparing the efficacy of these two blocks for postoperative analgesia in open radical retropubic prostatectomy and their effects on narcotic consumption.

NCT ID: NCT05611749 Not yet recruiting - Opioid Use Clinical Trials

Duloxetine Impact on Postoperative Pain Control and Outcomes

Start date: November 15, 2022
Phase: Phase 2
Study type: Interventional

1. Evaluate differences between patients taking Duloxetine or placebo following lateral lumbar interbody fusion for postoperative narcotic consumption. 2. Evaluate differences between patients taking Duloxetine or placebo following lateral lumbar interbody fusion for postoperative pain, function, and quality of life. 3. Evaluate the correlation between preoperative screening tests (measuring pain centralization, anxiety, depression, and overall function) and patients' response to treatment (reduction in pain, anxiety, or depression and improvement in function).

NCT ID: NCT05214157 Completed - Clinical trials for Cholecystectomy, Laparoscopic

Optimizing Pain Management Following Laparoscopic Cholecystectomy RCT

Pain
Start date: March 20, 2020
Phase: N/A
Study type: Interventional

evaluating the two final steps we added to optimize post laparoscopic cholecystectomy pain management.

NCT ID: NCT05021822 Completed - Clinical trials for Laparoscopic Cholecystectomy

The Effect of Erector Spinae Block on Diaphragma Movement

Start date: August 26, 2021
Phase: Phase 4
Study type: Interventional

Laparoscopic cholecystectomy surgeries cause moderate/severe pain and thus can result in shallow breathing, atelectasis and increased opioid consumption in the early postoperative period which in turn cause a longer hospital stay. Erector spinae plane block has been shown to decrease lower thoracic pain after laparoscopic cholecystectomy surgeries. This study aims to investigate the effect of erector spinae plane block on opioid consumption and diaphragma movement after laparoscopic cholecystectomy surgeries.

NCT ID: NCT04475198 Terminated - Clinical trials for Acute, Post-operative Pain

Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ST-2427

Start date: March 4, 2021
Phase: Phase 1
Study type: Interventional

This randomized, double-blind, placebo controlled, study will be conducted to evaluate the safety, tolerability, and pharmacokinetics of ST-2427. Subjects will be randomized to receive a single dose of ST-2427 or placebo in a Single Ascending Dose (SAD) design. A total of 30 subjects will be enrolled. Subjects will be randomized in a 4:2 ratio of ST-2427 to placebo. Study drug will be blinded to all subjects and investigators.

NCT ID: NCT01610882 Completed - Clinical trials for Acute Post-operative Pain

Panda: Evaluation of a Smartphone-based Perioperative Pain Assessment Tool

Panda
Start date: May 2012
Phase: N/A
Study type: Interventional

This study will evaluate Panda, a smartphone-based pain assessment tool. During a child's recovery from surgery, a Post-Anesthetic Care Unit nurse will assess their pain, which helps determine what medication they need. Traditionally, this involves asking the child to rate their pain on a scale from 1 to 10, by moving a slider along a coloured scale or pointing to one of a series of faces on a piece of card. The Panda uses the same methods, but presents them on a smartphone screen. Our evaluation will ensure that the Panda gives the same pain scores as the traditional methods.