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Pain, Postoperative clinical trials

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NCT ID: NCT04314570 Not yet recruiting - Pain, Postoperative Clinical Trials

Saphenous Nerve Block After Tibial Plateau ORIF

Start date: May 2025
Phase: N/A
Study type: Interventional

Fractures of the tibial plateau, while very painful, typically do not receive nerve blocks. This is because of a concern that the numbness from a nerve block would "mask" the typically painful symptoms of compartment syndrome, a condition that can lead to a permanent loss of function of the injured limb. Our study aims to evaluate the effectiveness of saphenous nerve block for pain management after surgical repair of a tibial plateau fracture. Based on cadaver studies and our clinical experience, we suspect that the saphenous nerve contributes to pain sensations of the tibial plateau and will not mask the pain from a compartment syndrome. In summary, while saphenous nerve block represents a safe option after tibial plateau open reduction internal fixation (ORIF), we aim to evaluate its effectiveness in this patient population.

NCT ID: NCT04313764 Not yet recruiting - Colorectal Cancer Clinical Trials

Ultrasound-Guided Erector Spinae Plan Block for Colorectal Surgery

Start date: June 18, 2020
Phase: N/A
Study type: Interventional

Colorectal cancer is a common and lethal disease. It still remains the third most common cause of cancer death in women and the second leading cause of death in men. Pain control is an important direction of postoperative management in malignancy surgery. Inadequate pain control increases cardiac and respiratory complications in these critical patients. Erector spinae plane (ESP) block is a recently described regional anesthesia technique that blocks the dorsal and ventral rami of the spinal nerves and the sympathetic nerve fibers. While the ESP block has been shown to provide effective postoperative analgesia after thoracic, and abdominal surgeries. Our aim in this study was to investigate bilateral thoracic ESP block for providing successful postoperative pain management following colorectal surgery.

NCT ID: NCT04307420 Not yet recruiting - Postoperative Pain Clinical Trials

Postoperative Pain Following Restoration With Composite Resin Versus Sonic Fill

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

The aim of this study is to assess the postoperative pain following restoration with composite resin versus sonic fill in children with deep carious first permanent molar.

NCT ID: NCT04296188 Not yet recruiting - Pain, Postoperative Clinical Trials

Erector Spina Plane Block vs Serratus Anterior Plane Block for Postoperative Mastectomy Pain

Start date: March 18, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare the efficiency of serratus anterior plane block and erector spina plane block on analgesic consumption, postoperative pain and patient's satisfaction and recovery quality in patients undergoing mastectomy.

NCT ID: NCT04259918 Not yet recruiting - Pain, Postoperative Clinical Trials

Effect of Alveolar Recruitment Maneuver on Postoperative Pain

Start date: February 25, 2020
Phase: N/A
Study type: Interventional

Control group: no additional procedure Low ARM group : recruitment maneuver of 30cmH2O High ARM group: recruitment maneuver of 60cmH2O

NCT ID: NCT04221685 Not yet recruiting - Pain, Postoperative Clinical Trials

Intraoperative Pain After Infiltration Technique Using Artpharma Versus Artinibsa in Children

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

The aim of this study is to assess Intraoperative pain for extraction of Maxillary primary molars using Artpharma Versus Artinibsa in children during infiltration technique.

NCT ID: NCT04190797 Not yet recruiting - Knee Osteoarthritis Clinical Trials

Photobiomodulation on Postoperative Pain

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

Objective: This study is designed to evaluate the short-term efficacy of photobiomodulation for improving pain and function in patients that will undergo total knee replacement and decrease in morphine consumption and adverse effects of opioids. Methods: thirty four patients of both genders that will undergo total knee replacement will participate in this randomized controlled double-blind clinical trial. They will be randomly allocated into two groups: Photobiomodulation group 1 with 18 patients and placebo group with 18 patients and group 3 control without device . Photobiomodulation will be performed twice during 48h, using adivice Light-Aid da BrightPhotomedicine- Brasil, com LED de Arsenieto, Gálio and Alumínio (AsGaAl) of 850 nm device 3B class, measured and calibrated previously .Five points were irradiated on the knee. The placebo group will be treated with the same laser device, but will not be turned on. All patients will receive treatment sessions of photobiomodulation after 24h and 48 h after peripheral nerve blockade (femoral nerve block and nerve supply), applied in 5 points for 5 minutes (300 seconds) close to the incision (that will be protected by transparent film) and repeated every 24h after totaling 2 applications. Patients will be assessed for duration of surgery and anesthesia, assessment of the pain, time to first rescue analgesia request, physical examination, dosimetry of photobiomodulation and amount of morphine consumption using PCA 24h and 48 hours after nerve blockade after surgery. In addition, adverse effects , sedation, paresthesias, motor blockade, nausea and vomiting will be assessed ever 6h during 48h.

NCT ID: NCT04177342 Not yet recruiting - Achalasia Clinical Trials

Post Operative Pain Control of POEM Procedure

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

Peroral endoscopic myotomy (POEM) is a minimally invasive treatment for esophageal achalasia with a natural orifice transluminal endoscopic procedure and far less invasive than the standard surgical or laparoscopic Heller myotomy (LHM). Less is known about the postoperative pain after POEM and the minor surgery trauma, short length of stay may lead to underestimation of postoperative pain control. We tend to observe the pain status after the POEM surgery under the empirical treatment in our center, and find a proper intra-operative way of pain control to solve the post-operative pain and seek the possible influence factors of postoperative pain.

NCT ID: NCT04176770 Not yet recruiting - Post Operative Pain Clinical Trials

Comparaison of ESP Block and TAP Block

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study aim to compare the efficiency and the analgesic effect of Erector Spinal Plane Block versus TAP Block after laparoscopic cholecystectomy.

NCT ID: NCT04151862 Not yet recruiting - Pain, Postoperative Clinical Trials

The Two Most Common Ways Post-operative Eye Patch Are Therapeutic Contact Lenses (TCL) and Overnight Bandaging With Tight Bandage Patch: This Study is Designed to Determine the Most Effective Post-operative Care to Relief the Patient's Discomfort After Pterygium Excision Surgery

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study is designed to determine the most effective post-operative care to relief the patient's discomfort after pterygium excision surgery.