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Pain, Postoperative clinical trials

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NCT ID: NCT03026530 Completed - Pain, Postoperative Clinical Trials

Effect of Pulmonary Recruitment Maneuver (PRM) on Pain and Nausea After Laparoscopic Bariatric Surgery

Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this prospective, blinded, randomized clinical trial is to investigate whether a ventilator-piloted PRM at the end of laparoscopic bariatric surgery could reduce overall postoperative pain and nausea.

NCT ID: NCT03023462 Completed - Pain, Postoperative Clinical Trials

Efficacy of an Anterior Quadratus Lumborum Block vs. a TAP-block for Inguinal Hernia Repair

Start date: September 5, 2019
Phase: N/A
Study type: Interventional

One of the most common complications after hernia repair is postoperative and chronic pain. TAP (transverse abdominis plain) block is a recommended multimodal method of reducing postoperative pain in laparoscopic and open inguinal hernia repair. The objective of this study is to determine whether the use of a perioperative echo guided unilateral TAP block has a superior effect on postoperative pain after laparoscopic inguinal repair compared to an anterior Quadratus Lumborum Block with a long acting local anesthetic.

NCT ID: NCT03021096 Completed - Pain, Postoperative Clinical Trials

Natural History of Pain After Shoulder Arthroplasty Conducted With Multimodal Analgesia

TSA Pain
Start date: January 27, 2017
Phase:
Study type: Observational

This study aims to identify the timeline of pain following total shoulder replacement with the goal of developing data for a subsequent randomized trial. The investigators believe that with using HSS's current protocol, many patients have postoperative pain that is no worse than their preoperative pain. Previous HSS anesthesia protocols for total shoulder arthroplasty patients have not formally followed patients past their hospital discharge, and the investigators believe that some patients do experience moderate to severe subacute postoperative pain. Therefore, this study's primary outcome is to look at the numeric pain scores at 14 days after surgery. Future studies will look at measures of preventing bruising and subsequent pain after shoulder replacement.

NCT ID: NCT03020966 Completed - Pain, Postoperative Clinical Trials

IV vs. Oral Acetaminophen as a Component of Multimodal Analgesia After Total Hip Arthroplasty

IV Tylenol
Start date: February 16, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine how well two different methods of administrating Tylenol reduce pain and improve patient satisfaction after total hip replacement (THR) surgery. The methods of administration are orally, via a pill that is to be swallowed, and intravenously. Our aim is to determine whether oral or intravenous administration of Tylenol will reduce opioid consumption and opioid-related side effects after THR.

NCT ID: NCT03019562 Recruiting - Pain, Postoperative Clinical Trials

Oxycodone vs. Fentanyl in Early Postoperative Pain After Total Hip Replacement

Start date: December 2016
Phase: Phase 4
Study type: Interventional

Oxycodone is one of the most widely used opioids for pain treatment. Many studies demonstrated good efficacy of oxycodone on postoperative pain. In this study, we assess the efficacy and side effects of bolus intravenous of oxycodone injection compared to those of fentanyl in patients after total hip replacement surgery.

NCT ID: NCT03018301 Recruiting - Postoperative Pain Clinical Trials

Intravenous Ketamine and Postoperative Pain Following Cesarean Section.

Start date: January 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the analgesic effect of low-dose intravenous ketamine in pregnant mothers undergoing cesarean section under Bupivacaine spinal anesthesia.

NCT ID: NCT03015987 Not yet recruiting - Necrosis Clinical Trials

Effect of Diode Laser Activated Irrigation Versus Ultrasonic on Post-Operative Pain in Single Visit of Necrotic Teeth

Start date: February 2017
Phase: N/A
Study type: Interventional

the investigator intended to study the effect of laser versus ultrasonic in activation of irrigation in post operative pain of patients have a symptomatic necrotic teeth

NCT ID: NCT03015961 Terminated - Clinical trials for Postoperative Pain Management

Phase 4, Controlled Study in Adult Subjects Undergoing Primary, 1-2 Level, Open Lumbar Spinal Fusion Surgery

Start date: February 21, 2017
Phase: Phase 4
Study type: Interventional

Primary Objective: The primary objective of this study is to compare postsurgical pain control following local infiltration analgesia (LIA) with EXPAREL admixed with bupivacaine HCl versus LIA with bupivacaine HCl in adult subjects undergoing open lumbar posterior spinal fusion surgery. Secondary Objectives: The secondary objectives of this study are to compare additional efficacy, safety, and health economic outcomes following LIA with EXPAREL admixed with bupivacaine HCl versus LIA with bupivacaine HCl in adult subjects undergoing open lumbar posterior spinal fusion surgery.

NCT ID: NCT03015532 Completed - Postoperative Pain Clinical Trials

Total Knee Arthroplasty Infiltration Study for Postoperative Analgesia

Start date: January 13, 2017
Phase: Phase 2
Study type: Interventional

This is a Phase 2b, randomized, double-blind, saline placebo- and active-controlled, multicenter study in subjects undergoing primary unilateral total knee arthroplasty (TKA) to evaluate the analgesic efficacy, safety, and pharmacokinetics (PK) of HTX-011 administered via infiltration to the surgical site.

NCT ID: NCT03011905 Completed - Pain, Postoperative Clinical Trials

Rebound Pain After Operations for Distal Radius Fractures With a Volar Plate in Brachial Plexus Block

Start date: January 2017
Phase: Phase 3
Study type: Interventional

Many patients have strong pain at brachial plexus block resolution after operations for distal radius fractures with a volar plate. This study investigates if a single dose of dexamethasone in addition to a standard pain regime have an effect on postoperative pain. The primary endpoint is difference in the highest pain score first 24 hours after surgery. The investigators will also look at pain scores and analgesics consumption first few hours after surgery and at different times up to 2 years after surgery.