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Levobupivacaine clinical trials

View clinical trials related to Levobupivacaine.

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NCT ID: NCT06011746 Completed - Chronic Pain Clinical Trials

Adding Ketamine to Levobupivacaine in Paravertebral Block in Thoracotomy

Start date: August 30, 2023
Phase: Phase 4
Study type: Interventional

To evaluate the role of adding ketamine to levobupivacaine in PVB on acute and chronic pain in thoracotomy

NCT ID: NCT05816538 Not yet recruiting - Breast Cancer Clinical Trials

The Immune Response of Breast Cancer Patients Treated With Levobupivacaine Using Paravertebral or Superficial Chest Blocks

Start date: April 2023
Phase: N/A
Study type: Interventional

The use of regional anesthesia in breast surgery improves the postoperative outcome, reduces the development of infection, and weakens the perioperative immunosuppressive response associated with the response to surgical stress. The investigators hypothesize that the use of propofol / paravertebral anesthesia and analgesia will be accompanied by a decrease in serum proinflammatory cytokines and/or an increase in anti-inflammatory cytokines compared to propofol / PECS 2 anesthesia and analgesia. The research will be on 100 respondents divided into two groups. 0.5% levobupivacaine will be administered to both groups. Serum concentrations of pro- and anti-inflammatory cytokines, and lymphocyte subpopulations 1h before, 24h, and 48h after surgery will be measured. The investigators aim to compare the effect of propofol / paravertebral and propofol / PECS 2 anesthesia and analgesia on serum perioperative values of pro-inflammatory and anti-inflammatory cytokines to standardize protocols and apply the best method of perioperative analgesia in breast cancer surgery.

NCT ID: NCT04968392 Completed - Dexmedetomidine Clinical Trials

Single-shot Adductor Canal Block With Levobupivacaine and Dexmedetomidine in Total Knee Arthroplasty

Start date: March 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

Total knee arthroplasty surgery is associated with severe postoperative pain and adequate pain management is necessary for early postoperative mobilization and rehabilitation. Although good postoperative pain control may be achieved by continuous epidural anesthesia or femoral nerve block, both methods have adverse effects such as muscle weakness, which may delay postoperative mobilization.

NCT ID: NCT04697329 Completed - Postoperative Pain Clinical Trials

Local Infiltration With Levobupivacaine During Laparoscopic Cholecystectomy

Start date: December 3, 2020
Phase: Phase 4
Study type: Interventional

Randomized controlled trial on laparoscopic cholecystectomy. Interventional group: preincisional infiltration with levobupivacaine. Control group: no local infiltration. Postoperative pain with numeric rating scale is registered, besides other parameters like heart rate, blood pressure, rescue analgesia requirements, nausea and vomiting, etc.

NCT ID: NCT04397406 Completed - Dexmedetomidine Clinical Trials

Dexmedetomidine or Fentanyl as Additives to Epidural Levobupivacaine in Painless Labor

Start date: July 1, 2020
Phase: Phase 4
Study type: Interventional

Central neuraxial analgesia has been extensively used for labor analgesia and is currently the gold standard technique for pain control in obstetrics. The aim of the study will be to compare the role of dexmedetomidine or fentanyl as additives to epidural levobupivacaine in painless vaginal delivery as regard maternal analgesia and safety.

NCT ID: NCT04113720 Completed - Levobupivacaine Clinical Trials

Levobupivacaine vs Levobupivacaine + Dexmedetomidine Infiltration for Post-tonsillectomy Analgesia and Laryngospasm in Pediatric Patients

Start date: November 15, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Tonsillectomy is one of the most common surgical performed procedures in children. Adenotonsillectomy surgery in pediatrics is commonly managed as an ambulatory surgery. This may be attributed to the use of the electro-dissection surgical technique that decreases the incidence of immediate postoperative hemorrhage. However, the use of the electro-cautery technique increases postoperative inflammation. Postoperative throat pain is a very important and significant problem because it can lead to decreased oral intake and dehydration with subsequent serious complications of dehydration.

NCT ID: NCT03919916 Recruiting - Pain Clinical Trials

Serratus Plane Block With Parenteral Opioid Analgesia Versus Patient Controlled Analgesia in Rib Fractures

COPE
Start date: May 28, 2021
Phase: N/A
Study type: Interventional

In this multicentre randomised controlled trial, adult patients with isolated chest trauma and two or more unilateral rib fractures will be randomised to either serratus plane block and patient controlled analgesia or patient controlled analgesia alone. Our primary outcome is the static visual analogue scale score at one hour.