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Anesthesia, Conduction clinical trials

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NCT ID: NCT05954689 Not yet recruiting - Hypertension Clinical Trials

Femoral Artery Block for Reduction of Tourniquet Induced Hypertension

Start date: July 10, 2023
Phase: N/A
Study type: Interventional

A randomised controlled trial to assess the impact of femoral artery block on the incidence of tourniquet hypertension in patients receiving cruciate ligament surgery with > 30 minutes of tourniquet under combined anaesthesia (balanced general anaesthesia and femoral nerve blocks).

NCT ID: NCT05749367 Not yet recruiting - Clinical trials for Anesthesia, Conduction

Lateral Cutaneous Nerve and PENG Blocks Versus Suprainguinal Fascia Iliaca Block in Post-op Analgesia of Hip Fractures

Start date: March 6, 2023
Phase: N/A
Study type: Interventional

Postoperative pain in hip fractures is challenging and requires adequate management. Peripheral nerve blocks are already known as superior than systemic analgesia in this scenario, but the best analgesic regional technique is still unknown. The investigators propose a study to compare the postoperative analgesia of hip fractures between pericapsular nerve group block plus lateral femoral cutaneous nerve block and suprainguinal fascia iliaca block

NCT ID: NCT04784104 Not yet recruiting - Pain, Postoperative Clinical Trials

Comparison of Infraclavicular And Supraclavicular Block

Start date: March 5, 2021
Phase: Phase 4
Study type: Interventional

Ultrasound-guided brachial plexus blocks are used successfully for upper extremity surgeries. In this randomized prospective single-blind study, ASA I-II patients aged 18-65 years undergoing hand, wrist, and forearm surgery will be randomly divided into two groups. First group will receive ultrasound-guided coronal oblique supraclavicular block using a 22G, 50 mm stimulator needle, and the second group, ultrasound-guided lateral sagittal infraclavicular block using a 22G 100 mm stimulator needle. We will prepare, 30 ml of 1:1 0.5% bupivacaine and 2% prilocaine with 5 mcg adrenaline per milliliter as local anesthetic mixture. Block application time, block success, sensory and motor block levels, and postoperative analgesia time will be recorded and compared between the groups. Accordingly, the success rate of the two methods will be evaluated.

NCT ID: NCT04768764 Not yet recruiting - Pain, Postoperative Clinical Trials

Comparison Of Femoral Block And Middle Adductor Canal Block In Patients With Knee Arthroplasty

Start date: April 16, 2021
Phase: Phase 4
Study type: Interventional

Femoral and adductor nerve blocks with ultrasonography(USG) guidance are used effectively and efficiently in post-operative pain management in lower extremity surgical procedures. However, the superiority of these two blocks to each other is still controversial. In this prospective, randomized, double-blind study, patients who underwent elective unilateral knee arthroplasty under spinal anesthesia, will be performed postoperative femoral block or middle adductor canal block with the guidance of USG.Patients who underwent spinal anesthesia and needed sedoanalgesia and who had to switch to general anesthesia will be excluded from the study. The patients will be divided into two groups by simple randomization. Since a total of 52 patients should be included in the study as a result of the power analysis (G-power 3.1); It is planned to take approximately 26 patients for each group.The anesthesiologist, who follows the pain control and mobilization after the block, will not know which study group the patient is in. The blocks will be performed behind the cover while the patient is under spinal anesthesia (Thus, the point of application of the block will not be noticed). In this way, the patient and the anesthesiologist who follows the parameters after the block will be blind to patient's arm. In the first group, 0.25% 20 ml of local anesthetic and middle adductor canal block, in the second group 0.25% 20 ml of local anesthetic and femoral nerve block will be applied We will compare these two blocks in terms of early mobilization, postoperative pain control, motor, and sensory block.

NCT ID: NCT04294537 Not yet recruiting - Laparoscopy Clinical Trials

TAP Block or Wound Infiltration for Laparoscopic Pediatric Appendectomy: a Pilot Study

Start date: March 30, 2020
Phase: N/A
Study type: Interventional

Effectiveness of the TAP block compared to wound infiltration in controlling pain after laparoscopic appendectomy in children