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Analgesia clinical trials

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NCT ID: NCT06202430 Active, not recruiting - Analgesia Clinical Trials

Ultrasound Guided Block for Postoperative Analgesia in Arthroscopic Shoulder Surgery

Start date: August 13, 2023
Phase: N/A
Study type: Interventional

This study aimed to compare the efficacy of high thoracic-ESPB with shoulder block as analgesic options for arthroscopic shoulder surgery. Primary outcome: • 24-hour analgesic consumption. Secondary outcomes: - Postoperative pain evaluated by: Visual Analogue Pain Scale (VAS). - Time to first rescue analgesia and total postoperative consumption of analgesia. - Effect of the block on Hemodynamics. - Adverse effects in the form of postoperative nausea and vomiting (PONV). - Patient satisfaction.

NCT ID: NCT06125067 Active, not recruiting - Analgesia Clinical Trials

Fascia Iliaca Compartment Block and iPACK Block in Total Knee Arthroplasty

Start date: June 10, 2023
Phase:
Study type: Observational

The investigators sought to compare the effectiveness of postoperative pain control between the standard intravenous multimodal analgesia procedure used in managing patients undergoing total knee surgery, who experience severe postoperative analgesia needs, and multimodal analgesia procedures that incorporate ultrasound-guided peripheral nerve blocks (Fascia Iliaca Compartment Block or iPACK Block) during postoperative follow-up. The aim is to determine which procedure is more effective.

NCT ID: NCT06058715 Active, not recruiting - Analgesia Clinical Trials

TAP Block Versus Conventional Systemic Analgesia

TAPLAP
Start date: September 15, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare TAP block to conventional systemic analgesia for postoperative pain management in patients undergoing elective laparoscopic cholecystectomy. As the adverse effects of pain management is related to size of opioid dose use, opioid consumption is chosen as the primary outcome and a decrease of at least 20% in the TAP block compared with the conventional systemic analgesia is considered to be clinically significant. Written informed consent has to obtained from all study patients. This trial is a prospective parallel group randomized superiority trial comparing TAP block to classic systemic analgesia in patients undergoing elective laparoscopic surgery in the department of surgery, Mahmoud El Matri Hospital, Ariana, with a 1:1 allocation ratio.

NCT ID: NCT05763810 Active, not recruiting - Analgesia Clinical Trials

Comparing Different Regional Blocks for Analgesia After Off-pump Cardiac Surgery

Start date: March 15, 2023
Phase: N/A
Study type: Interventional

This study aims to compare the analgesic effects of erector spinae plane block versus Superficial Parasternal Intercostal Plane Block block along with rectus sheath block after off-pump cardiac surgery

NCT ID: NCT05439343 Active, not recruiting - Analgesia Clinical Trials

Adductor Canal Block and Multimodal Local Infiltration Analgesia in Patients Receiving Total Knee Arthroplasty

Start date: October 15, 2018
Phase: N/A
Study type: Interventional

Total knee arthroplasty (TKA) is associated with moderate to severe pain after operation. There are twenty thousand patients undertaking TKA annually in Taiwan, and the average length of hospital stay is about seven to ten days. In contrast, the length of hospital stay is only three to six days in some literatures. Adequate pain relief after surgery allows patients to mobilize earlier and easier and rehabilitate to reduce the length of hospital stay. By reducing hospital stay, we can reduce medical expenditure of national health insurance. In addition, effective analgesia can reduce the occurrence of chronic post-surgical pain which would compromise life quality and produce socioeconomic problems. This study tries to find a better solution for postoperative analgesia of TKA for patients in Taiwan. The present clinical study compares the effect of adductor canal block and local infiltration on postoperative analgesia and functional activity after TKA. To assess the outcome of both methods in the same patient, we can have more comparative result of pain score and functional parameters like range of motion of knee joint, time and ability to ambulate. Based on that, we try to find a better option for postoperative analgesia for patients receiving TKA in Taiwan.

NCT ID: NCT05109312 Active, not recruiting - Analgesia Clinical Trials

A Multi-surgery Assessment of ZYNRELEF (HTX-011), AMAZE. Master Protocol HTX-011-401.

Start date: October 12, 2021
Phase: Phase 4
Study type: Interventional

This is a Phase 4, randomized, blinded, active-controlled, multicohort study to evaluate HTX-011 compared with bupivacaine HCl in subjects undergoing different surgical procedures. Each parallel cohort will enroll subjects undergoing a unique surgical procedure: total shoulder arthroplasty (TSA) in Cohort 1 and abdominoplasty in Cohort 2.

NCT ID: NCT04866368 Active, not recruiting - Postoperative Pain Clinical Trials

Comparison of Erector Spinae Plane Block and Penile Block in Hypospadias Surgery

Start date: April 20, 2021
Phase: N/A
Study type: Interventional

In this study, we aimed to compare ultrasound-guided sacral erector spinae plane block and dorsal penile block on postoperative analgesic effect in hypospadias surgery.

NCT ID: NCT04852484 Active, not recruiting - Pain, Postoperative Clinical Trials

Morphine Versus Ketamine as Adjuvants in Paravertebral Blocks

Annie-Dimitr
Start date: April 16, 2021
Phase: N/A
Study type: Interventional

The aim of this study will be to compare the effects of morphine versus ketamine when they are used as adjuvants to the local anesthetic in paravertebral nerve blocks performed with the aid of ultrasound. Furthermore, a group of local anesthetic without an adjuvant, will also be compared to the two groups

NCT ID: NCT04732234 Active, not recruiting - Analgesia Clinical Trials

Pre-emptive US Guided Superior Hypogastric Plexus Block in Pelvic Cancer Surgeries : a Randomized Double-Blinded Study

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

The superior hypogastric plexus (SHP) is a retroperitoneal structure with a predominance of afferent sympathetic nerve fibers. The perception of central pelvic pain is thought mainly to involve transmission through this plexus. Therefore, blocking or of SHP has been used to treat pelvic pain.

NCT ID: NCT04675671 Active, not recruiting - Anxiety Clinical Trials

Analgesic and Anxiety Efficacy of Preemptive Pregabalin

Start date: December 1, 2019
Phase:
Study type: Observational [Patient Registry]

Effective postoperative pain control after arthroscopic shoulder surgery optimizes postoperative rehabilitation, reduces anxiety, and can increase patient satisfaction and postoperative healing by providing amnesia and sedation. Few literature is available for postoperative pain management, including intra-articular local anesthetic infiltration, regional nerve blocks, patient-controlled analgesia (PCA) with intravenous opioid, and oral nonsteroidal anti-inflammatory and gabapentinoid drugs. Recently, gabapentinoides such as pregabalin have also shown to have potential in the treatment of acute postoperative pain as part of multimodal analgesia, due to their possible opioid consumption-reducing effects and prevention of post-surgical chronic pain. Pregabalin is an anticonvulsant drug that reduces calcium entry into the nerve terminals of the central nerve and also reduces levels of substance P, glutamate and noradrenaline, all of which play a major role in creating a feeling of pain. It is well known that pregabalin reduces central sensitization and hyperalgesia after tissue injury by inhibiting calcium influx in voltage-gated calcium channels. These theoretical advantages have led to clinical trials to confirm the analgesic effectiveness of oral pregabalin for postoperative pain management in various surgical procedures.