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Postoperative Pain clinical trials

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NCT ID: NCT03695367 Completed - Postoperative Pain Clinical Trials

Phase 2 Herniorrhaphy Study for Opioid Elimination

Start date: October 1, 2018
Phase: Phase 2
Study type: Interventional

This is a Phase 2, open-label study in subjects undergoing unilateral open inguinal herniorrhaphy.

NCT ID: NCT03693222 Completed - Postoperative Pain Clinical Trials

Quadratus Lumborum Block in Pediatric Patients

Start date: May 15, 2016
Phase: N/A
Study type: Interventional

Quadratus lumborum block (QLB) is a newly-defined trunk block performed with local anesthetic injection by imaging the abdominal muscles with ultrasonography (US) guidance; thus, analgesia is expected to be ensured from the T7-L1 dermatomal segment level. In the study, the aim was to compare the postoperative analgesic effect of quadratus lumborum block in pediatric patients undergoing lower abdominal surgery

NCT ID: NCT03692546 Completed - Postoperative Pain Clinical Trials

Liposomal Bupivacaine for Pain Control After Rotator Cuff Repair

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

The use of an interscalene block (ISB) is often associated with rebound pain that could be avoided through adjunctive therapy with longer duration. Administration of a liposomal bupivacaine (LB) field block in addition to ISB would overcome this rebound pain to provide greater pain relief and reduce opiate consumption when compared to ISB alone. 50 patients were recruited and randomized into groups that either received or did not receive an intraoperative LB field block in addition to standard ISB administration. Visual Analog Scale (VAS) pain scores and narcotic consumption were recorded over the five-day postoperative period to determine the effectiveness of LB pain relief.

NCT ID: NCT03692286 Completed - Postoperative Pain Clinical Trials

Assessment of Postoperative Pain After Using Various Intracanal Medication in Patients With Necrotic Pulp

Start date: June 1, 2019
Phase: Phase 4
Study type: Interventional

To assess the Postoperative Pain after using Silver Nanoparticles with and without Calcium Hydroxide as an Intracanal Medication in Patients with necrotic pulp (RCT)

NCT ID: NCT03685396 Completed - Postoperative Pain Clinical Trials

Patient Morbidity After Palatal Free Gingival Grafts With or Without PRF Membranes Coverage

Start date: November 27, 2017
Phase: N/A
Study type: Interventional

This study evaluates postoperative morbidity of patients that undergo free gingival graft harvesting from palate with or without use of autogenous PRF (Platelet Rich Fibrin) membranes to cover the donor site.In the Test Group venous blood sampling was done in order to prepare PRF membranes used to cover the donor site, whereas in Control Group hemostatic agents with oxidized and regenerated cellulosa were used.

NCT ID: NCT03685370 Recruiting - Pancreatic Cancer Clinical Trials

PERiX: Comparison of Efficacy Between Placement of Epidural Catheters X-ray Guided and LOS Technique

PERiX
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

The use of epidural catheters for postoperative analgesia in pancreatic surgery is recommended by the guidelines of the ERAS society. Some studies claim it may expose to hemodynamic alterations that may compromise outcome and increase postoperative complications, attributable to a malfunction of the catheter itself, often linked to a bad positioning, since this is usually positioned with LOS technique. Our hypothesis is that a positioning made using the radiographic guide the day before the intervention can significantly reduce the number of catheter's dysfunctions.

NCT ID: NCT03680716 Completed - Postoperative Pain Clinical Trials

Combined Saphenous Nerve and IPACK Blocks Versus Infiltration Analgesia After Anterior Cruciate Ligament Reconstruction

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

A lot of patient have posterior knee pain after ACL reconstruction despite saphenous nerve block. Recently a new block has been described, know as IPACK block (interspace between the popliteal artery and the capsule of the posterior knee). The objective of this randomized controlled double-blinded trial is to assess whether a combined saphenous nerve block with IPACK block is more effective for the postoperative pain than a local infiltration analgesia.

NCT ID: NCT03678168 Completed - Pain Clinical Trials

A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries

Start date: September 5, 2018
Phase: N/A
Study type: Interventional

Post-operative, throat pain, nausea and vomiting is a common occurrence in rhinology surgeries due to the use of throat packs during the procedure. In order to optimize quality of care and patient satisfaction, the aim of this study to evaluate the incidence of post-operative, throat pain, nausea and vomiting in patients that have been packed with either conventional gauze throat packs or pharyngeal tampons.

NCT ID: NCT03677817 Completed - Postoperative Pain Clinical Trials

Perioperative Lidocaine Administration in Thoracoscopic Surgery for Improved Postoperative Pain Control

Start date: April 3, 2019
Phase: Phase 3
Study type: Interventional

Placebo-controlled study to analyze the effect of perioperative intravenous lidocaine administration on total morphine consumption (TMC) and on pain intensity in thoracoscopic surgery .

NCT ID: NCT03675386 Recruiting - Chronic Pain Clinical Trials

Reducing Opioid Use for Chronic Pain Patients Following Surgery

RECOUP
Start date: September 24, 2018
Phase: N/A
Study type: Interventional

Patients with chronic pain are often prescribed long-term opioid therapy, despite the serious risks and growing concerns related to opioid use. The Toronto General Hospital has created the world's first multidisciplinary perioperative Transitional Pain Service Program (TPSP) aimed at reducing the incidence and severity of chronic post-surgical pain. The TPSP incorporates a variety of mechanisms and interventions to help patients manage pain and to wean off opioids. The approach consists of: pain education, Acceptance and Commitment Therapy (ACT), and an e-mobile self- management tool to help patients manage chronic pain more effectively. With the TPSP team, the investigators hope to continually assist patients to achieve a balance between the benefits and potential harms of opioid use to promote long-term health and well-being.