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Pain, Postoperative clinical trials

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NCT ID: NCT03950700 Completed - Teeth, Impacted Clinical Trials

Bupivacaine in the Treatment of Postoperative Pain of Impacted Third Molar Extraction

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

The third molars are the teeth that are most frequently included and impacted, extraction is one of the most performed treatments by maxillofacial surgeons in their clinical practice. Its surgical extraction is accompanied by an inflammatory process, which generates pain, edema and trismus. The use of alternatives that offer prolonged analgesia, like the use of bupivacaine, reduce the pain of the patient after an extraction of third molars, allows the reduction of morbidity and the rapid return to daily activities. In addition, it allows a better experience in the dental consultation. Investigators hypothesis is: Irrigation of the alveolus with 4 ml of 0.5% bupivacaine is effective for the reduction of post-operative pain in extraction of impacted lower third molars

NCT ID: NCT03947372 Completed - Pain, Postoperative Clinical Trials

Comparison of Outcomes After Laparoscopic Versus Open Appendectomy in Acute Appendicitis

Start date: February 21, 2015
Phase: N/A
Study type: Interventional

A comparison study was performed between laparoscopic appendectomy and open appendectomy in acute setting in tertiary hospital to access the outcome of postoperative pain and hospital stay. As the popularity of laparoscopic appendectomy has failed in major tertiary hospital due to huge amount of patient load in which open appendectomy was performed.This study was performed to prove that outcome of laparoscopic appendectomy are far better than open appendectomy and to increase the use of laparoscopic surgery in acute settings

NCT ID: NCT03946982 Completed - Clinical trials for Post-cesarean Pain Control Quality

Comparisons Between Low Thoracic and Lumbar Epidural Analgesia on Postoperative Pain Low Thoracic v.s. Lumbar Epidural for Post-cesarean Pain

Start date: May 28, 2019
Phase: N/A
Study type: Interventional

Whether low thoracic epidural analgesia improves postoperative cesarean pain qualities than conventional lumbar epidural analgesia?

NCT ID: NCT03946306 Completed - Pain, Postoperative Clinical Trials

Evaluation of Postoperative Pain With Eddy Tips (EPPET)

Start date: February 13, 2020
Phase: N/A
Study type: Interventional

This investigation will focus on the use of EDDY tips, because it is known that the complete debridement of the canal is very difficult, which leads to an accumulation of tissue debris, bacteria and their products, resulting in persistent periradicular inflammation. So, it's of great importance, the study of other approaches of cleaning and disinfecting the root canal, which at the same time, may produce a lower risk of postoperative pain. The above mentioned topics have never been analysed simultaneously with the use of EDDY tips, and the evaluation of the postoperative pain was never addressed. This research is of great clinical interest, due to the complexity of root canal system, with isthmuses, ramifications and dentinal tubules, that make the total elimination of bacteria impossible, even with the best clinical protocols, because the irrigants cannot penetrate the dentinal tubules, and the postoperative pain is an exhausting factor for patients. Therefore, a new protocol, with better disinfection rate and less postoperative pain, will be able to increase the success rate of endodontic treatments, allowing to save condemned teeth.

NCT ID: NCT03944291 Completed - Pain, Postoperative Clinical Trials

Pudendal Nerve Block for Post-Episiotomy Pain Relief

Start date: May 1, 2019
Phase: Phase 3
Study type: Interventional

Unilateral vs. Bilateral Pudendal Nerve Block for Post-Episiotomy Pain Relief: A Randomized Clinical Trial

NCT ID: NCT03942237 Completed - Pain Management Clinical Trials

Transmuscular Quadratus Lumborum Block for Postoperative Pain After Laparoscopic Adrenalectomy

Start date: May 10, 2019
Phase: N/A
Study type: Interventional

This prospective, randomized control study aims to compare the analgesic effect, satisfaction with anesthesia and analgesia between single-injection QLB (quadratus lumborum block)+general anesthesia (GA) and general anesthesia (GA) alone in patients undergoing laparoscopic adrenalectomy.

NCT ID: NCT03942107 Completed - Postoperative Pain Clinical Trials

Postoperative Pain After Dental Post Application

Start date: April 5, 2019
Phase: N/A
Study type: Interventional

In this study the effect of dental post application on postoperative dental pain in patients with asymptomatic teeth after a single-appointment root canal treatment will be evaluated.

NCT ID: NCT03941899 Completed - Postoperative Pain Clinical Trials

The Analgesic Effect of QLB II After Robotic Prostatectomy. (QLB II: Quadratus Lomborum Block II Type)

QLBII
Start date: May 6, 2019
Phase: N/A
Study type: Interventional

The analgesic effects of Quadratus Lomborum Block II type after robotic-assisted laparoscopic radical prostatectomy, will be assessed.

NCT ID: NCT03936387 Completed - Pain, Postoperative Clinical Trials

Bilateral Continuous Erector Spinae Blocks for Post-Sternotomy Pain Management: A Pilot Study

Start date: July 1, 2019
Phase: Phase 3
Study type: Interventional

Overall Aim: To evaluate the feasibility and potential benefits of investigating bilateral continuous erector spinae blocks (BESB) for postoperative pain management in a small cohort of children undergoing surgical sternotomy prior to planning an appropriately powered, randomized, controlled trial of the same. Hypothesis: The investigators' primary hypothesis is that utilizing bilateral erector spinae blocks for post-sternotomy pain is a feasible intervention for consideration in a larger trial by demonstrating a 75% or greater successful intervention completion rate without any major adverse outcomes.

NCT ID: NCT03935412 Completed - Postoperative Pain Clinical Trials

The Analgesic Efficacy of Bilateral Erector Spinae Plane Block in Comparison With Intrathecal Morphine After Elective Cesarean Section

Start date: March 5, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to assess the analgesic efficacy of bilateral erector spinae plane block in comparison with intrathecal morphine after elective cesarean section under spinal anesthesia.