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Chronic Postoperative Pain clinical trials

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NCT ID: NCT04313855 Completed - Clinical trials for Chronic Postoperative Pain

Help With Early Detection of Postoperative Neuropathic Pain Using SMS After Ambulatory Surgery

SMS DPpostop
Start date: December 9, 2020
Phase: N/A
Study type: Interventional

Chronic post-operative pain is generally defined by persistent pain more than 2 months after surgery. General reviews on chronic post-operative pain describe an overall incidence of 30%, of which 5 to 10% are described as severe. Different risk factors have been identified: pain and preoperative opioid use, anxiety - depression, catastrophism, type of surgery, intensity and duration of postoperative pain, genetic factors. If postoperative pain is essentially pain caused by excess nociceptive stimulation, investigators realize that a neuropathic component is far from being exceptional and that this can be demonstrated quickly after surgery. In addition, these neuropathic pains respond little or no to the usual analgesics and in particular to opioids, which can be the cause of misuse or death from overdose. Early detection of pain of a neuropathic nature would allow appropriate therapy to be put in place and may therefore reduce the risk of chronic postoperative pain. The concept of ambulatory surgery assumes that postoperative pain will be minimal and can be controlled at home by the administration of oral pain relievers. However, following the development of surgical techniques and the improvement in the quality of care, the number and complexity of procedures that can be performed in ambulatory surgery have increased considerably. Consequently, a significant number of patients will probably develop chronic post-operative pain without the possibility of early detection. The prevalence of chronic post-operative pain in ambulatory surgery has been studied by a single team. The authors conclude that it is underestimated and variable depending on the surgery between 15 and 32%. For the past few years, the GHPSJ has been using an ambulatory surgery algorithm that sends SMS messages to warn and follow up on patients. The principle is simple: patients scheduled for outpatient surgery receive text messages the day before their intervention to remind them of the instructions to be followed and the meeting times and, the day after the operation, the algorithm sends SMS to ask patients if all is well or if they have pain, nausea or vomiting, discharge from the scar. In postoperative monitoring, this technology has shown promising results. This technology has not been used in the screening of persistent pain. The objective of this work is to assess the effectiveness of an SMS algorithm in the early detection of postoperative neuropathic pain after surgery performed on an outpatient basis.

NCT ID: NCT04280432 Completed - Clinical trials for Cesarean Section Complications

Monocentric Observational Study: Postoperative Pain After Cesarean Section: Incidence and Risk Factors.

Start date: March 1, 2017
Phase:
Study type: Observational

The purpose of this prospective study was to assess chronic pain 3, and 12 months after cesarean delivery in a cohort of women in University hospital La Paz. We also aim to study the possible contribution of anesthetic and surgical risk factors for the development of Chronic post-surgical pain after cesarean (PCSCP)

NCT ID: NCT03529201 Completed - Pain, Postoperative Clinical Trials

QLB After Nephrectomy

Start date: May 7, 2018
Phase: N/A
Study type: Interventional

Oxycodone consumption and postoperative pain intensity in patients undergoing nephrectomy procedures. Of all study participants, 50% will obtain quadratus lumborum block (QLB).

NCT ID: NCT02630849 Completed - Clinical trials for Chronic Postoperative Pain

Does a Multimodal no‐Compression Suture Technique of the Intercostal Space Reduce Chronic Post‐Thoracotomy Pain?

Start date: October 2011
Phase: N/A
Study type: Interventional

Chronic post-thoracotomy pain is a significant adverse outcome of thoracic surgery. transcollation technology evaluated with a prospective randomized trial the effect of a multimodal no-compression suture technique of the intercostal space on postoperative pain occurrence in patients undergoing mini-thoracotomy. Patients undergoing a muscle-sparing lateral mini-thoracotomy for different thoracic diseases were randomly divided into two groups:one group received intercostal muscle flap harvesting and pericostal no-compression "edge" suture (IMF group), and the second group received a standard suture technique associated with an intrapleural intercostal nerve block (IINB group). The aim of the study was to demonstrate that the multimodal no-compression suture technique is a rapid and feasible procedure reducing early and chronic post‐thoracotomy pain intensity.

NCT ID: NCT02190682 Completed - Clinical trials for Chronic Postoperative Pain

Data Collection for Prediction of Postoperative Chronic Pain for a Software

Start date: October 2014
Phase:
Study type: Observational [Patient Registry]

Postoperative Persistent Pain (PPP) is reported with a high incidence in adults 11.5-47%. This high incidence effects quality of life of patients causes social-economical problems and arises medico-legal issues. This study will be undertaken for producing a database by the evaluation of surgeries in 4 hospitals located in Istanbul. This database will be used in establishing a software by using data mining technology in the prediction of PPP

NCT ID: NCT02137135 Completed - Clinical trials for Chronic Postoperative Pain

Menstrual Phase and Postoperative Pain

Start date: August 2012
Phase: Phase 0
Study type: Interventional

Fluctuations of female sex hormones during the menstrual cycle influence pain perception. Endogenous pain is pronounced in the follicular phase of the menstrual cycle. The investigators tested the primary hypothesis that the women having surgery during their follicular phase have more acute pain and require more opioids than those in the luteal phase, and secondarily the investigators tested that women who have surgery during their follicular phase have more incisional pain at 3 month postoperatively.

NCT ID: NCT02115945 Completed - Clinical trials for Chronic Postoperative Pain

Femoral and Epidural Block After Total Knee Arthroplasty

Start date: February 2013
Phase: Phase 0
Study type: Interventional

Total knee prosthetic replacement causes severe postoperative pain. Various analgesic techniques have been used in pain control. Comparison of epidural and femoral nerve block is lacking, furthermore effect on chronic pain is unclear. The investigators aimed to compare the effects of epidural and femoral block on acute and chronic postoperative pain.

NCT ID: NCT01510496 Completed - Clinical trials for Chronic Postoperative Pain

Transition From Acute to Chronic Pain After Inguinal Hernia, Hysterectomy and Thoracotomy: Analysis of Risk Factors and Association With Genetic Polymorphisms

Start date: January 2009
Phase: N/A
Study type: Observational

The treatment of postoperative pain continues to be inadequate in the investigators practice setting. Inadequate pain treatment not only contributes to postoperative complications in the short term but can also be a factor that favors the development of chronic postoperative pain and diminishes long-term quality of life. Risk factors that can lead to a transition to chronic pain need to be analyzed.

NCT ID: NCT01467102 Completed - Clinical trials for Chronic Postoperative Pain

euCPSP: European Observational Study on Chronic Post Surgical Pain,PAIN-OUT Study

PAIN-OUT
Start date: July 2011
Phase: N/A
Study type: Observational

This project a European observational study on the incidence and characteristics of chronic post surgical pain (CPSP). Research Questions - What is the incidence of chronic post surgical pain (CPSP) in Europe? - What are the risk factors of chronic post surgical pain (CPSP) related to surgery, patient and anaesthesia management? - What are the difference in incidence and risk factors in different European countries?

NCT ID: NCT01388946 Completed - Pain, Postoperative Clinical Trials

Analgesia in Laparoscopic Cholecystectomy

Start date: May 2010
Phase: N/A
Study type: Interventional

The investigators hypothesis is that perioperative infusion of 0.75 ropivacaine in patients undergoing laparoscopic cholecystectomy may modify the intensity of postoperative pain or the analgesic consumption during the first 24 hours.