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Acute Pain clinical trials

View clinical trials related to Acute Pain.

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NCT ID: NCT04967118 Recruiting - Pain, Acute Clinical Trials

Neonatal Pain Management and Pain Monitoring Using New Methods

Start date: May 2, 2023
Phase: N/A
Study type: Interventional

The aim of this randomized controlled study with crossover design is to examine the effectiveness of mother-driven interventions, skin-to-skin contact (SSC) and recorded mother's heartbeats as sound and vibration (MHB), compared to oral glucose in relieving neonatal acute pain related to heel lance as a painful procedure. The effectiveness of interventions will be assessed using validated pain scales (PIPP-R and NIAPAS), changes in sensory cortex activation (near-infrared spectroscopy, NIRS) and changes in physiological indicators (oxygen saturation, heart rate, respiratory rate). The secondary objectives will include evaluating the effectiveness of interventions in relation to infant recovery and evaluating the use of NIRS monitoring in relation to neonatal pain assessment scales.

NCT ID: NCT04892901 Recruiting - Acute Pain Clinical Trials

Erector Spinae Plane Block in Uniportal VATS

ESPB-UVATS
Start date: January 1, 2022
Phase:
Study type: Observational

The main aim of this study is to compare the effectiveness of three alternative techniques (continuous Erectus Spinae Plane Block : c-ESPB; continuous Serratus Anterior Plane Block : c-SAPB; and Intercostal Nerve Block: ICNB) in reducing the severity of early postoperative pain after Uniportal-VATS lung resections. Primary outcomes will be opioid and other analgesic drugs consumption in the 72 hours after surgery, and static and dynamic pain scores, measured by the visual analog scale (VAS), at 6 pre-established time-points during the first 48 hours postoperatively. Further outcomes will be incidence of pulmonary and cardiac complications until patient's discharging, pain when removing drains, presence/absence of chronic neuropathic pain (12 weeks after surgery).

NCT ID: NCT04883034 Recruiting - Acute Pain Clinical Trials

Adductor Canal Block in Outpatient Clinic for Pain Control After Knee Arthroplasty

ACB
Start date: June 1, 2020
Phase: N/A
Study type: Interventional

Single-shot Adductor Canal Block in the outpatient clinic is safe, significantly decreased pain and analgesic consumption and may enhance the rehabilitation program

NCT ID: NCT04879004 Recruiting - Pain Clinical Trials

EFFECT - EFFectiveness of ESPB (Erector Spinae Plane Block) in Laparoscopic Cοlectomies Trial

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

The aim of the trial is to study the efficacy of continuous bilateral Erector Spinae Plane Block (ESPB) in managing perioperative pain in patients who undergo elective laparoscopic colectomy.

NCT ID: NCT04858711 Recruiting - Pain, Postoperative Clinical Trials

Opioid-free Anesthesia With a Mixture of Dexmedetomidine-lidocaine-ketamine

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

The aim of this study will be to investigate the effect of an opioid-free anesthesia regimen with a mixture of dexmedetomidine-lidocaine-ketamine in the same syringe versus fentanyl analgesia in elective laparoscopic gynecological surgery

NCT ID: NCT04849455 Recruiting - Anesthesia Clinical Trials

Erector Spinae Plane Block Catheters and Intrathecal Morphine for Hepatic Resection

Start date: May 24, 2021
Phase: Phase 4
Study type: Interventional

To determine whether the addition of erector spinae plane (ESP) catheters to existing multimodal analgesic regimen with intrathecal morphine provides superior postoperative analgesia in patients undergoing hepatic resection compared with patients not receiving ESP catheters.

NCT ID: NCT04829409 Recruiting - Pain, Acute Clinical Trials

The Effects of Three Different Ultrasound-guided Nerve Blocks in VATS

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

Ultrasound-guided mid-point transverse process to pleura block, erector spinae plane block and paravertebral block are three different methods of nerve block, used for relieving postoperative pain in thoracic anesthesia. This study is to compare them on block effects, postoperative pain and analgesic consumption in video-assisted thoracic surgery.

NCT ID: NCT04787198 Recruiting - Pain, Acute Clinical Trials

Investigating Composite Biomarkers for Pain Catastrophizing

Start date: October 15, 2022
Phase: N/A
Study type: Interventional

Pain is a complex, multidimensional, and subjective experience; and although, investigators use a single word "pain", to describe our perception, multiple mechanisms contribute to the generation and maintenance of pain. To help diagnosing and improving pain management, there is a need for developing tools. These tools may include measurements of substances, or biomarkers, in the blood; e.g. small molecules called microRNA and proteins. In these experiments, the investigators would like to investigate how the psychological response to stress and pain alters the impulses in the brain and the content of microRNA and proteins in the blood. The future aim is to identify patients in high risk of developing and maintaining chronic pain and to be able to treat chronic pain efficiently.

NCT ID: NCT04774783 Recruiting - Chronic Pain Clinical Trials

Pilot Study on the Effects of Low-Level Laser Therapy Treatment for Acute and Persistent Discomfort

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

This study will examine the effectiveness of Low-Level Laser Therapy (LLLT) for the management of pain in various locations of the body. All subjects selected for participation in the study will be assigned to a LLLT treatment group for a duration of 12 sessions.

NCT ID: NCT04750031 Recruiting - Pain, Acute Clinical Trials

Pain Scores and Complications do Not Differ at Three Recovery Position After Liver Biopsy

Start date: January 1, 2018
Phase:
Study type: Observational

Liver biopsy is still used as the gold standard in the diagnosis of many liver diseases. During the observation after liver biopsy, patients are hospitalized on their right side, which is the biopsy side, with the thought that adverse events (complications) such as bleeding or bile leakage will be less. Patients who do not develop complications after 4-6 hours of observation are discharged home. Some of the patients state that the right side-lying position for 4-6 hours is uncomfortable than the biopsy itself, and they prefer to lie on their back. In our study, researchers aim to investigate the rate of complications after biopsy, what recovery position found more acceptable by the patients.