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Pain, Postoperative clinical trials

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NCT ID: NCT05062356 Recruiting - Clinical trials for Chronic Postoperative Pain

Pain Control Following Total Hip Arthroplasty

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

Total hip arthroplasty (THA) is one of the most common surgical procedures performed in elderly patients, with its main indication being end-stage osteoarthritis of the hip1. It is estimated that over 572,000 patients per year will undergo THA in the USA alone by 20301 and postsurgical pain associated with THA remains a significant issue. Postoperative pain is associated with delayed joint mobilization, ambulation, patient satisfaction and can often delay the patient's discharge home1. Multimodal analgesia for the management of postoperative pain following THA is now standard of care2,3. It involves a combination of local anesthetic infiltration (LAI), peripheral nerve blocks (PNBs), analgesics such as non-steroidal anti-inflammatory drugs (NSAIDs), acetaminophen and/or other medications, including gabapentinoids and opioids. Using multiple analgesic modalities allows for an easier and faster recovery for THA patients and ultimately allows for reduction in postoperative narcotic use and it's associated negative side effects. Total hip arthroplasty can be performed under either general anesthesia, epidural anesthesia or most commonly under spinal anesthesia, with or without epidural morphine. The adjunctive use of LAI, pericapsular nerve group (PENG) block or suprainguinal fascia iliaca compartment block (FICB) for postoperative pain management is becoming more widespread, although evidence on their efficacy has been inconsistent4-8. As such, comparative evaluation of these adjuctive analgesic modalities is imperative to optimize postoperative pain management following THA.

NCT ID: NCT05058287 Recruiting - Pain, Postoperative Clinical Trials

Lumbar Steroid Use in Patients Undergoing Posterior Lumbar Decompression

Start date: November 5, 2021
Phase: Phase 3
Study type: Interventional

This study seeks to evaluate the impact of intra-operative topical epidural steroid usage in patients undergoing 1-2 level lumbar laminectomy. The study will examine post-operative opioid usage, length of stay, return to work, and patient reported outcomes following these procedures.

NCT ID: NCT05044858 Recruiting - Postoperative Pain Clinical Trials

Ultrasound-Guided Mid-Point Transverse Process to Pleura Block for Thoracotomy Incisions

Start date: September 24, 2021
Phase: N/A
Study type: Interventional

This study is designed to investigate the analgesic efficacy of pre-emptive ultrasound-guided midpoint transverse process to pleura (MTP) block for posterolateral thoracotomy in cardiothoracic surgeries.

NCT ID: NCT05044247 Recruiting - Pain, Postoperative Clinical Trials

The Effect of Both Ultrasound and Fluoroscopy Guide Erector Spinae Plane Blocks

Start date: April 20, 2021
Phase: N/A
Study type: Interventional

Since the original publication on the erector spinae plane (ESP) block in 2016, the technique of the ESP block has evolved significantly in the last few years. Current reports suggest that the ESP block provides adequate analgesia in thoracic and abdominal sites in a post-surgical and chronic pain patient. However, there were still inconsistencies and unclear spread of local anesthetics in ultrasound guide ESP block. This study focusing on the spread of local anesthetic in ESP block under ultrasound and fluoroscopy and possible mechanisms of action.

NCT ID: NCT05037123 Recruiting - Clinical trials for Chronic Postsurgical Pain

Optimizing the Use of Ketamine to Reduce Chronic Postsurgical Pain

KALPAS
Start date: January 4, 2022
Phase: Phase 3
Study type: Interventional

The study utilizes a 3-arm placebo-controlled RCT to study the effectiveness of ketamine in reducing chronic post-mastectomy pain. Participants randomized to the first arm will receive a 0.35 mg/kg dose after induction, followed by a 0.25 mg/kg/hr infusion during surgery (up to a maximum of 6 hours) and continued for 2 hours postoperatively. Participants in the second arm will receive a single dose of 0.6 mg/kg of ketamine in the post-anesthesia care unit, and the final group will serve as the control group and receive saline (no ketamine).

NCT ID: NCT05021809 Recruiting - Clinical trials for Necrotic Pulp With Symptomatic Apical Periodontitis

Assessment of Postoperative Pain After Using Two Formulations of Calcium Hydroxide Intracanal Medication .

Start date: July 25, 2021
Phase: Phase 4
Study type: Interventional

Calcium hydroxide is advocated as an intracanal medication for various purposes, including prevention of post-treatment symptoms. Calcium hydroxide has a pain-controlling effect at different times when compared to non-intracanal medication . Aim: The aim of the study to compare between postoperative pain after using two formulations of calcium hydroxide intracanal medication with and without iodoform .

NCT ID: NCT05011084 Recruiting - Cryotherapy Effect Clinical Trials

Combined Cryotherapy With Compression Versus Cryotherapy Alone After Orthopaedic Surgery

Start date: November 2, 2020
Phase: N/A
Study type: Interventional

Cryotherapy has been used to enhance recovery after orthopaedic surgery. Many devices are available but few can guarantee a temperature regulation during a prolonged time and therefore have been criticized. The arrival of new advanced cryotherapy devices made it possible to test the effect of prolonged cooling on rehabilitation after arthroscopic orthopaedic procedures.

NCT ID: NCT05009771 Recruiting - Postoperative Pain Clinical Trials

Postoperative Pain Management of Caesarean Section

Start date: February 23, 2022
Phase:
Study type: Observational

Caesarean section is one of the most frequent surgeries causing severe postoperative pain. Poor management of acute pain can contribute to postoperative complications, late recovery and the development of chronic pain. Moreover, it had been demonstrated that the intensity of postpartum pain is associated with depression. It is imperative to find out appropriate methods of postpartum pain alleviation. Currently, a lot of analgesic drugs and methods have been developed and used in clinical practice, such as patient-controlled analgesia, extended-release analgesics and multimodal analgesia. This prospective cohort study is aimed to investigate the outcome of each postoperative analgesic method used in caesarean section.

NCT ID: NCT05008614 Recruiting - Postoperative Pain Clinical Trials

Comparison of Continuous ESP Versus TEA After Thoracotomy

Start date: July 22, 2021
Phase: N/A
Study type: Interventional

This prospective, randomized, assessor-blinded study is designed to evaluate the postoperative analgesic efficacy of the ultrasound-guided continuous erector spinae plane (ESP) block in patients undergoing thoracotomy. We hypothesize that US-guided ESP block is not inferior to thoracic epidural analgesia in terms of postoperative pain control in these patients.

NCT ID: NCT05003765 Recruiting - Clinical trials for Post-operative Pain Management

Are Superficial Parasternal Intercostal Plane (SPIP) Blocks With Bupivacaine and With or Without Adjuvants Helpful for Post-operative Pain After Coronary Artery Bypass Grafting?

Start date: August 6, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the addition of the superficial parasternal intercostal plane (SPIP) block alone (30cc of 0.25% bupivacaine) or plus Magnesium (200mg of magnesium sulfate) or plus Magnesium + Buprenorphine (300mcg) as adjuvants can improve post-operative pain in patients undergoing cardiothoracic surgery, specifically, coronary artery bypass grafting (CABG)