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Nerve Block clinical trials

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NCT ID: NCT04715880 Completed - Pain, Postoperative Clinical Trials

The Comparison of the Analgesic Efficacy and Hemodynamic Effects of Paravertebral Block Compared With Paravertebral and Intercostal Nerve Block for Thoracotomy in Adults.

Start date: February 15, 2021
Phase: N/A
Study type: Interventional

Thoracotomy is a surgical procedure associated with severe post operative pain during the first day of surgery and is responsible for prolonged hospital stay, patient dissatisfaction and delayed return to normal activities along with increased morbidity and mortality. Investigators intend to compare the efficacy of two analgesic interventions (continuous infusion of paravertebral block (PVB) after loading dose compared with intercostal nerve block and continuous infusion of PVB without loading dose) on postoperative thoracotomy pain. The results of this study will direct the investigators to find the best practice methods which will reduce the postoperative thoracotomy pain, the overall cost of pain management and length of patient's hospital stay.

NCT ID: NCT04675372 Completed - Nerve Block Clinical Trials

Dexmedetomidine Facilitate Analgesia

Start date: January 19, 2021
Phase: Phase 4
Study type: Interventional

Pre-clinic evidences showed that DEX produces antinociception by inhibiting the activation of spinal microglia and astrocyte decreasing noxious stimuli evoked release of nociceptive substances and further interrupting the spinal neuron-glia cross talk and regulating the nociceptive transmission under chronic pain condition. in this study, the analgesic efficacy of Dexmedetomidine was evaluated by a new non-invasive nociceptive index (qNOX). In this study, Anagel6000 analgesia monitor was used to quantitatively compare the analgesic efficacy of Dexmedetomidine compared with Midazolam.

NCT ID: NCT04633850 Completed - Lung Cancer Clinical Trials

Implementation of Adjuvants in Intercostal Nerve Blockades for Thoracoscopic Surgery in Pulmonary Cancer Patients

Start date: September 8, 2020
Phase:
Study type: Observational

To investigate the effect of intercostal blockade with and without adjuvants.

NCT ID: NCT04471025 Completed - Nerve Block Clinical Trials

Jedi Grip Versus Double Operator Technique For Ultrasound Guided Infraclavicular Block

Start date: May 14, 2018
Phase: N/A
Study type: Interventional

The investigators aimed to compare the block characteristics of the single operator "jedi grip" technique and the conventional double operator technique.

NCT ID: NCT04451642 Completed - Clinical trials for Postoperative Complications

A Retrospective Clinical Registry of Peripheral Nerve Block

Start date: January 1, 2011
Phase:
Study type: Observational

Locorregional anaesthesia have been increased its role in different kind of surgeries, alone or combined with general anesthesia. Due to ultrasound, peripheral nerve blocks have been increased their importance in locoregional anaesthesia. They provide excellent intraoperative and postoperative analgesia, decreasing the need for intravenous opioids which increase postoperative nausea and vomiting which may prolong hospital stay. The primary study objective is to analyze retrospectively the use of peripheral nerve blocks in the current practice of a specialized regional anaesthesia division. This is an observational, retrospective and unicenter study. 1346 patients scheduled for the surgery needed a peripheral nerve block were enrolled.

NCT ID: NCT04426500 Completed - Pain, Postoperative Clinical Trials

Use of Perioperative Pain Blocks In Urological Surgery

Start date: November 11, 2019
Phase: Phase 3
Study type: Interventional

The study team aims to prospectively compare Placebo (local administration), ultrasound-guided transversus abdominis plane (UTAP) blocks, and laparoscopic-guided transversus abdominis plane (LTAP) blocks in patients undergoing robotic surgery of the prostate and kidney. The study team expects to be able to equally efficiently administer the blocks using direct visualization and ultrasound guidance. The study team expects that a negative result would obviate the need for longer operative time by eliminating the need for the separate ultrasound guided block while a positive result would demonstrate the increased utility of preoperative ultrasound blocks in managing postoperative pain.

NCT ID: NCT04356521 Completed - Anesthesia, Local Clinical Trials

Lateral Sagittal vs Costoclavicular Approach for Ultrasound-Guided Infraclavicular Block

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

An ultrasound-guided infraclavicular block performed with the costoclavicular (CC) approach and the lateral sagittal (LS) approach will be compared in patients scheduled for forearm and hand surgery.

NCT ID: NCT04298775 Completed - Nerve Block Clinical Trials

Postoperative Urinary Retention in Orthopedic Patients

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to compare the incidence of postoperative urinary retention related to spinal anesthesia with morphine and spinal anesthesia associated with peripheral blockade in orthopedic procedures of lower limbs. Secondary objectives are assessing the incidence of nausea and vomiting; postoperative pain and opioid consumption at 24 hours after surgery with each of the techniques. A total of 52 patients submitted to a lower limb orthopedic procedure were randomized to the intervention groups: spinal anesthesia with morphine versus spinal anesthesia without opioid associated with peripheral nerve block. After surgery, bladder ultrasound will be performed in post-anesthesia care unit to identify urinary retention and patients will be followed for 24 hours to assess outcomes.

NCT ID: NCT03982784 Completed - Pain Management Clinical Trials

TQLB for Postoperative Pain After Laparoscopic Partial Nephrectomy

Start date: June 10, 2019
Phase: N/A
Study type: Interventional

This prospective, randomized study,control study aims to compare the analgesic effect,opioids consumption,quality of recovery,length of hospital stay,et al. between single-injection QLB(quadratus lumborum block)+ intravenous patient-controlled analgesia (IPCA) and intravenous patient-controlled analgesia (IPCA) alone in patients undergoing laparoscopic partial nephrectomy.

NCT ID: NCT03942237 Completed - Pain Management Clinical Trials

Transmuscular Quadratus Lumborum Block for Postoperative Pain After Laparoscopic Adrenalectomy

Start date: May 10, 2019
Phase: N/A
Study type: Interventional

This prospective, randomized control study aims to compare the analgesic effect, satisfaction with anesthesia and analgesia between single-injection QLB (quadratus lumborum block)+general anesthesia (GA) and general anesthesia (GA) alone in patients undergoing laparoscopic adrenalectomy.