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Postoperative Pain clinical trials

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NCT ID: NCT04579354 Completed - Anxiety Clinical Trials

Virtual Reality (VR) Tour to Reduce Preoperative Anxiety Before Anaesthesia

VR OP- tour
Start date: September 7, 2020
Phase: N/A
Study type: Interventional

Anxiety and apprehension are common among patients prior to surgery. This anxiety can lead to additional discomfort, increased pain sensation and increased stress symptoms. Virtual exposure has proven to be successful in exposure therapy for the treatment of the narrowest patients. Patients are not confronted with the real stimuli or situations that trigger the branches, but with virtual representations of them. Virtual reality (VR) makes it possible to create scenarios that would not be possible in reality because of the organisational, time or financial expenditure involved.The effectiveness of virtual stimulus exposure is well documented, especially in the case of object or situation-related fears in the context of specific phobias. It is therefore obvious that virtual stimulus exposure could also be suitable for minimising operation-associated fears.The research project described is designed to investigate the effect of virtual stimulus exposure on perioperative anxiety. For this purpose, a virtual tour of the operating setting has been created, which enables patients to explore the surroundings in detail by means of VR glasses.

NCT ID: NCT04578483 Not yet recruiting - Postoperative Pain Clinical Trials

Postoperative Pain Management of Therapeutic Surgery: a Prospective, Observational Cohort Study.

Start date: October 26, 2020
Phase:
Study type: Observational [Patient Registry]

Poor management of post-operative acute pain can contribute to medical complications including pneumonia, deep vein thrombosis, infection and delayed healing, as well as the development of chronic. In contrast, appropriate pain control is capable of reducing the postoperative complications, preventing the development of chronic pain, and improving the quality of life. The workloads of medical staffs and health care cost are subsequently decreased. Recently, a lot of analgesic methods have been developed and used in clinical practice, such as patient-controlled analgesia, ultrasound-guided long-term analgesia and multimodal analgesia. This study is aimed to investigate the outcome of each postoperative analgesic method used in China Medical University Hsinchu Hospital. This real world data can serve as a reference toward high health care quality.

NCT ID: NCT04574154 Completed - Postoperative Pain Clinical Trials

Regional Anesthesia in THR - Comparing the Analgesic Efficacy of Fascia Iliaca Block and Erector Spinae Plane Block

PTA-ALR
Start date: January 20, 2020
Phase: N/A
Study type: Interventional

THR (Total Hip Replacement) can be very painful and regional anesthesia is very effective in reducing postoperative pain. Fascia Iliaca Block (FIB) and Erector Spinae Plane Block (ESPB) are indirect approaches to the lumbar plexus that resulted to be very promising for THR. However, no studies investigated the analgesic superiority of either FIB or ESPB. In our study the investigators compare FIB and ESPB in terms of pain relief expressed as morphine consumption in the first 24 hours after primary THR.

NCT ID: NCT04571515 Completed - Pain Clinical Trials

Dose-Response Study of MR-107A-01 in The Treatment of Post-Surgical Dental Pain

Start date: September 29, 2020
Phase: Phase 2
Study type: Interventional

MR-107A-01 is being studied to investigate its efficacy, safety, and dose-response after dental surgery.

NCT ID: NCT04567407 Completed - Postoperative Pain Clinical Trials

Bilateral Continuous Erector Spinae Blocks for Post-Sternotomy Pain Management

Start date: September 22, 2020
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy of bilateral continuous erector spinae blocks (BESB) for postoperative analgesia in children and adolescents undergoing cardiac surgical procedures via sternotomy in the Early Recovery After Surgery (ERAS) program in a single arm, open label, interventional study.

NCT ID: NCT04564963 Active, not recruiting - Postoperative Pain Clinical Trials

The Effect of Intermittent Cryotherapy Exposure on Patients' Quality of Recovery After Surgery

ICE
Start date: October 5, 2021
Phase: N/A
Study type: Interventional

"Cryotherapy", or cold therapy, can include the use of gel packs, ice bags, ice baths, whole body chambers, and cold aerosol sprays. It is a popular non-drug treatment that can be used after a surgical operation, along with medication such as narcotics and anti-inflammatories for pain management. The application of ice packs on areas of injury has been used for many decades, as they can decrease both inflammation and pain. Other possible benefits include reduced blood flow, swelling, and tissue damage as well as muscle spasms. While there is some evidence to suggest that the use of ice packs is beneficial, this has not yet been implemented into practice, nor do any guidelines recommend the use of ice packs for pain management in surgical patients. In this trial, adult patients undergoing scheduled thoracoabdominal or groin surgery will be randomly assigned to apply ice packs over the largest closed surgical incision every 4 hours, at minimum, for 72 hours (while the patient is awake), along with standard of care, or to receive standard of care only. This trial will be conducted under the IMPACTS (Innovative, Multicentre, Patient-centred Approach to Clinical Trials in Surgery) program umbrella and will follow IMPACTS methodology. For the Vanguard trial, the aim is to determine the feasibility of conducting a definitive trial. Future outcomes of interest are quality of patient recovery, pain, length of hospital stay and medication use.

NCT ID: NCT04561856 Not yet recruiting - Postoperative Pain Clinical Trials

Fascia Iliaca Block Supplemented With Perineural Vs Intravenous Dexamethasone

Interventional
Start date: September 30, 2020
Phase: Phase 4
Study type: Interventional

Split-thickness skin grafting is the current standard of care for the reconstructive procedures in managing burn injuries and traumatic tissue defects. Harvesting split-thickness skin creates a new partial thickness wound that is referred to as the donor site . Donor site pain is one of the most distressing symptoms reported by patients in the early postoperative period. Larger donor sites stimulate a greater number of pain receptors and consequently pain is proportional to the size of the graft harvested.Often, the donor site is reported to be more painful than the recipient site,affecting early mobilization, sleep, and need for analgesics postoperatively.

NCT ID: NCT04559438 Completed - Postoperative Pain Clinical Trials

Post-operative Pain Following Glide Path Preparation Using Rotary Neoniti GPS File and Manual K-files

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to clinically compare the incidence of post-operative pain after using rotary glide path file (Neoniti GPS), on post-operative pain when compared to manual glide path preparation in lower molars with asymptomatic non-vital pulp.

NCT ID: NCT04555993 Recruiting - Postoperative Pain Clinical Trials

Erector Spinae vs TAP in Lower Abdominal Surgery

Start date: February 28, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare the analgesic effect and safety profile of erector spinae plane block with transverses abdominis plane block in controlling peri-operative pain for lower abdominal cancer surgery.

NCT ID: NCT04554862 Completed - Postoperative Pain Clinical Trials

The Analgesic Efficacy of Magnesium and Ketorolac in Ultrasound Supraclavicular Block

Start date: October 1, 2019
Phase: Phase 4
Study type: Interventional

Despite many regional anesthetic techniques have been described for anesthesia of the brachial plexus which is responsible for the sensory and motor innervation of entire upper limb, still, supraclavicular block (SCB) is the regional anesthetic technique of choice. SCB has been described as the spinal anesthesia of the upper limb as it offers dense anesthesia of the brachial plexus for the surgical procedures below the arm from elbow to hand. Although the SCB has a high incidence of complications like pneumothorax, the use of ultrasound-guided block improved the safety for the patient. There are several adjuvants have been added to SCB aiming for prolongation of the duration of peripheral nerve block as fentanyl, alpha 2 adrenergic agonist (Dexmedetomidine, Clonidine), tramadol, ketorolac and Magnesium sulfate. Magnesium has anti-nociceptive effects in animal and human models, principally related to blocking the N-methyl-D-aspartate (NMDA) receptors and regulation of calcium influx into cells. Calcium influx leads to a sequence of central sensitization such as windup phenomenon and long term potentiation which are crucial mechanisms that determine the duration and intensity of post-operative pain. Magnesium prevents central sensitization triggered by peripheral nociceptive stimulation in response to painful stimuli. Non-Steroidal Anti-Inflammatory drugs (NSAID) inhibit synthesis of prostaglandins from arachnoid acid in phospholipid membranes resulting in decreased afferent nociceptive signals from the site of surgery. There are a lot of studies supported the analgesic effect when NSAIDs are concentrated at a peripheral site compared to the systemic administration therapy. Ketorolac is a parenteral NSAIDs. Studies have shown that ketorolac as an adjuvant to local anesthetics during peripheral nerve block enhanced duration and quality of analgesia.