Clinical Trials Logo

Regional Anesthesia clinical trials

View clinical trials related to Regional Anesthesia.

Filter by:

NCT ID: NCT04764591 Completed - Regional Anesthesia Clinical Trials

Tissue Perfusion for Different Approaches of Brachial Plexus Block

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

To compare the two different approaches of infraclavicular brachial plexus block in forearm, wrist and hand surgery in terms of perfusion index, tissue oxygenation, sensory and motor block onset time and total effect time, first analgesic time, side effects and complications, and duration of block application.

NCT ID: NCT04733781 Not yet recruiting - Clinical trials for Musculoskeletal Pain

Subcutaneous Injection of Large Volumes of Tumescent Lidocaine and Epinephrine by Laypersons

TLE-RCT
Start date: February 22, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

This research is intended to show that it is safe and not difficult for nearly anyone to inject at least 125ml of a dilute solution of tumescent lidocaine and epinephrine (TLE), where a TLE solution consists of lidocaine (1gm/L) and epinephrine (1mg/L) in normal saline.

NCT ID: NCT04706780 Terminated - Regional Anesthesia Clinical Trials

Hemi-diaphragmatic Paresis After Erector Spinae Plane Block

Start date: January 20, 2021
Phase:
Study type: Observational [Patient Registry]

To assess the incidence of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane (ESP) block

NCT ID: NCT04700943 Completed - Thoracic Surgery Clinical Trials

Ultrasound Assessment of Diaphragmatic Dysfunction in Regional Anesthesia

Start date: February 1, 2019
Phase:
Study type: Observational

Awake thoracic surgery is a feasible and safe alternative to general anesthesia for pulmonary biopsy in interstitial lung disease patients, but there is still no evidence as to its superiority in terms of outcome. However, there is extensive literature about the effect of anesthetic drugs and surgery on diaphragmatic function. Furthermore, in thoracic surgery, diaphragmatic dysfunction was associated with a higher occurrence of postoperative pulmonary complications. To assess the impact of general anesthesia on diaphragmatic function, the investigators conducted an observational prospective trial. The investigators measured both diaphragmatic excursion and Thickening Fraction at baseline and 12 hours after surgery together with pulmonary function tests and gas exchange data.

NCT ID: NCT04677348 Completed - Hip Fractures Clinical Trials

Comparison of PENG Block and FICB in Hip Fracture Patients

Start date: January 21, 2021
Phase: N/A
Study type: Interventional

Fascia iliaca compartment block (FICB) has been considered the block of choice for patients with hip fracture. However, pericapsular nerve group (PENG) block, one of the relatively newly-developed blocks, could be also used for analgesia in patients with hip fracture. Since PENG block could block the accessory obturator nerve, PENG block might have greater analgesic effects compared to FICB theoretically. However, the comparison of these two blocks in patients with hip fracture has not performed in clinical setting. Thus, we aimed to compare the analgesic effect of PENG block and FICB.

NCT ID: NCT04670497 Completed - Regional Anesthesia Clinical Trials

Perioperative Analgesia for Total Hip Arthroplasty

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

This study is comparing the effect of lumbar plexus block and fascia iliaca block with general anesthesia to provide perioperative pain control and compare their effects on hemodynamics

NCT ID: NCT04668183 Completed - Regional Anesthesia Clinical Trials

Ultrasound-guided PNB and DPNB for Pediatric Distal Hypospadias Surgery

Start date: November 1, 2019
Phase:
Study type: Observational

Hypospadias repair is a urological surgical operation that is very painful in the postoperative period and requires long-term analgesia. A dorsal penial nerve block (DPNB) and pudendal nerve block (PNB), which are regional anesthesia techniques for this operation, are used to provide postoperative analgesia.

NCT ID: NCT04642612 Terminated - Regional Anesthesia Clinical Trials

Cerebral Blood Flow Evaluation With Trancranial Doppler After Interscalene Nerve Block

CBF-TCD
Start date: March 4, 2021
Phase:
Study type: Observational

The purpose of this study is to assess cerebral blood flow velocity (CBFV) following regional anesthesia for shoulder surgery. The results of this study will help to further understand the physiologic effect of the interscalene nerve block on cerebral blood flow.

NCT ID: NCT04629612 Not yet recruiting - Pain Clinical Trials

Regional Anesthesia in Breast Surgery

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

There is a trend that breast surgery can be done with peripheral nerve blockade and intravenous sedation, which reduces the side effects of general anesthesia such as nausea and vomiting, intubation discomfort and postoperative pain. The distribution of breast nerves is complex. Common nerve block methods are paravertebral blocks and pectoral nerve blocks. By monitoring the patient's heart rate variability change and measuring the patient's parasympathetic tone, the analgesic drug can be administered according to the patient's individual differences to avoid insufficient or excessive analgesic dose. The aim of this proposal is a prospective randomized controlled clinical trial is designed to evaluate changes in analgesia nociception index (ANI), surgical pleth index (SPI), postoperative opioid demand, and pain scores between patients who received regional anesthesia and those without in breast surgery patients under non-intubated surgery.

NCT ID: NCT04551833 Not yet recruiting - Regional Anesthesia Clinical Trials

Tramadol Versus Dexamethasone as Adjuvant to Levobupivacaine Supraclavicular Block

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

The investigator's aim will be to compare the efficacy of perineural tramadol and dexamethasone added to levobupivacaine in prolonging postoperative analgesia in patient undergoing open reduction and internal fixation for forearm fractures. Primary outcome: duration of postoperative analgesia. Secondary outcome: include [The anesthesia onset time, total rescue analgesic consumption in the 1st 24-hour and the presence of complications and side effects.