Clinical Trials Logo

Chronic Postoperative Pain clinical trials

View clinical trials related to Chronic Postoperative Pain.

Filter by:

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: NCT03363672 Not yet recruiting - Clinical trials for Chronic Postoperative Pain

Prevalence, Impact and Predictors of Chronic Postoperative Pain

Start date: January 1, 2018
Phase: N/A
Study type: Observational [Patient Registry]

Chronic postoperative pain (CPP) remains a disturbing and obscure clinical problem, which could last for more than 3 months after surgery. The aim of present study was to assess the prevalence of CPP, investigate its impact on life quality and explore its potential risk factors. After informed consent was signed, patients receiving surgery under general anesthesia in Peking Union Medical College Hospital and other medical centers participating in this study during 2018 will be included. Patients' preoperative information will be collected from medical record, including basic demographic data, primary disease and previous chronic diseases. Intraoperative information will be obtained from anesthesia record, including surgical scope, duration, length and location of incisions and blood loss. Acute pain will be evaluated in the ward of the department of surgery, when an app will be installed on patients' mobile phones. Our long-term postoperative follow-up would be performed by sending out survey questionnaires via this app in the 4th, 8th, 16th, 32th, and 48th weeks after surgery. The survey covers questions regarding the intensity, characteristic, location and impact on daily activities of CPP. Information regarding treatment of CPP will also be collected, if any. All the data gained will be summarized in our database and analyzed.

NCT ID: NCT03275207 Not yet recruiting - Clinical trials for Chronic Postoperative Pain

Dexmedetomidine for Prevention of Chronic Postoperative Pain

Start date: January 1, 2018
Phase: Phase 4
Study type: Interventional

Chronic postoperative pain (CPSP) is common symptom in patients after surgery, seriously affected the quality of life. Accumulating evidences have demonstrated dexmedetomidine can improve chronic pain. However, the prevention of dexmedetomidine on CPSP remain uncertain.

NCT ID: NCT02991287 Not yet recruiting - Clinical trials for Chronic Postoperative Pain

Validation of Predictive Scale of Chronic Postsurgical Pain

Start date: February 2017
Phase: N/A
Study type: Observational

To asses the precision of a score to predict chronic post surgical pain in patients undergoing inguinal hernia repair, abdominal hysterectomy, vaginal hysterectomy and thoracotomy. Prospective multicenter cohort study in 21 hospital in spain.

NCT ID: NCT02924519 Active, not recruiting - Clinical trials for Chronic Postoperative Pain

Postoperative Pain After Ambulatory Arthroscopic Shoulder Surgery

Start date: May 2014
Phase: N/A
Study type: Observational

Shoulder disorders are frequent, often associated with pain and occur in 7-34% of the general population and in 21% of the elderly population. Of particular interest is prediction of postoperative pain after outpatient arthroscopic shoulder surgery since the clinical experience is that surgery does not always provides pain relief and the interindividual variation in acute postoperative pain intensity is significant. In addition, a Swedish study has shown that shoulder operations are associated with longer convalescence than other orthopaedic outpatient surgeries.

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.