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Pain, Postoperative clinical trials

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NCT ID: NCT03706352 Completed - Post Operative Pain Clinical Trials

Is Tunneling Effective in Preventing Failure of Epidural Analgesia? A Randomized Trial

Start date: April 14, 2015
Phase: N/A
Study type: Interventional

This is a prospective randomized single blinded study in patients planned to undergo general anesthesia and epidural catheter insertion for pain control after abdominal, thoracic and orthopedic surgery. Patients meeting participation criteria will be selected and enrolled sequentially. The study recruitment will be carried out over one year with follow-up for each patient until either the catheter is dislodged or once decided that the patient is to be discontinued from the epidural pain control.

NCT ID: NCT03706313 Completed - Post-operative Pain Clinical Trials

Genicular Nerve Block for Total Knee Arthroplasty

Start date: January 15, 2019
Phase: Phase 4
Study type: Interventional

This study seeks to examine the analgesic efficacy of genicular nerve blocks for pain after total knee replacement.

NCT ID: NCT03704961 Completed - Pain, Postoperative Clinical Trials

Effect of Auditory Distractions on Pediatric Postoperative Pain

Start date: January 2017
Phase: N/A
Study type: Interventional

The aim of the study was to determine the effect of different auditorial methods of attention distraction on postoperative pain and anxiety in children. Three group pre and post-test randomized clinical trial.The data were collected using the Socio-demographic Data Form for Child and Parent, Visual Analogue Scale, Wong-Baker Faces Pain Scale and State-Trait Anxiety Inventory for Children. The investigators found that listening to classical music, Turkish music and audiobook methods played an effective role in decreasing postoperative pain and anxiety state in children in the three groups in the study. As a result, investigators showed that different auditorial attention distraction methods had a decreasing effect on postoperative pain and anxiety in children.

NCT ID: NCT03704753 Recruiting - Postoperative Pain Clinical Trials

New Truncal Nerve Blocks for Thoracoscopic Surgery and Open Heart Surgery.

Start date: January 25, 2019
Phase: Phase 4
Study type: Interventional

This study is divided to two sub-studies. First sub-study evaluates if Serratus Anterior Plane block (SAPB) reduces opioid consumption after thoracoscopic surgery. Secondly continuous SAPB is compared to continuous intercostal blockade. Second sub-study evaluates if Subpectoral Interfascial Plane block (SIP) reduces opioid consumption after medial sternotomy.

NCT ID: NCT03698565 Completed - Pain, Postoperative Clinical Trials

Evaluation of the Analgesia Nociception Index and Videopupillometry to Predict a Child's Post-tonsillectomy Morphine Prescription

ENIGME
Start date: December 20, 2018
Phase: N/A
Study type: Interventional

Some surgeries, such as tonsillectomies, are particularly painful postoperatively because they are not very accessible to a complementary technique of loco-regional anesthesia and require the use of opioids in the postoperative period. The use of opioids, in combination with usual analgesics, is common after this surgery. However, some risks are associated with the use of morphine in children, including more frequent respiratory distress, nausea and vomiting, and can cause hemorrhagic complications and lengthen the duration of hospitalization. Decreasing the consumption of morphine drugs is therefore a real challenge. Although there is no randomized controlled study on the use of standard analgesics with or without morphine to date, a number of studies suggest that the use of morphine should not be systematic after a surgery. The need for opioids after tonsillectomy as well as the level of pain vary between patients. Some teams use morphine at the end of general anesthesia to prevent pain on waking and others use it only if needed, once the child is awake. Pain assessment scales are used in the Post-interventional Monitoring Room (PIMR) to adapt these analgesic therapies according to the intensity of pain. One of the validated and frequently used scales in pediatric PIMR is FLACC (Face Legs Activity Cry Consolability). Monitoring tools are also available to evaluate the quality of intraoperative analgesia in unconscious children : - the analysis of the pupillary variation in response to a painful stimulus by videopupillometry, - and the ANI (Analgesia Nociception Index) which consists of estimating the sympathetic-parasympathetic balance by a complex analysis of cardiac rhythm variability. These two types of monitoring could predict which children will require post-operative morphine treatment. To date, no study has demonstrated the relationship between videopupillometry and postoperative morphine consumption. The average ANI has already been evaluated in children as correlated with FLACC but both monitoring devices have never been compared for a predictive purpose. The investigators hypothesize that the use of the PPI® (Pain Pupillary Index) scale of Algiscan® and the average ANI measured by the PhysioDoloris® monitor in children still sedated at the end of the intervention could have a prognostic value on post-operative morphine prescription.

NCT ID: NCT03697733 Completed - Clinical trials for Abnormal Uterine Bleeding

Comparison Efficiency of Oral Etoricoxib Versus Intravenous Fentanyl on Post Operative Pain in Curettage Under TIVA

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

Comparison of the efficiency of oral Etoricoxib versus intravenous Fentanyl on post operative Pain in curettage under TIVA: A randomized controlled trial

NCT ID: NCT03697278 Recruiting - Surgery Clinical Trials

Monitoring Postoperative Patient-controlled Analgesia (PCA)

Start date: September 28, 2018
Phase: N/A
Study type: Interventional

The introduction of Acute Pain Service (APS), 1985, specialized pain management could be offered to the inpatient care. An example of this is patient-controlled analgesia (PCA), which is a technique that is used mostly after surgery. A PCA pump is an electronic pump that is prepared with pain relief medicine, usually an opioid, which is administered either epidural or intravenously. PCA pumps are programmed with medical protocols. For prevent overdose, there are blocking times between possible bolus doses and a maximum dose per hour. In a Cochrane review from 2015, PCA have shown to be more beneficial for the patient especially when it comes to patient satisfaction, compared to conventional pain relief where nurses administer pain relief on request. The authors could also demonstrate that patients experience less pain and were more satisfied with patient-controlled analgesia. However, studies have showing limitations in the ease of practice of the PCA pumps, which indicates need for further development. Today the major part of the documentation in the Swedish healthcare is computerized. Using digital systems that communicate with each other should be seen as a matter of course. Instead, a human intermediator is commonly used where documentation is performed by pencil and paper. Due to the human factor that may affect the interpretation of the information the patient safety is placed at risk. The elimination of the human intermediator could lead to a safer transfer of information. There are already studies concerning computerized PCA pumps and wireless communication by medical devices, but only studies that are conducted outside of Europe and studies with the technical aspect in focus. Studies have shown that wireless communication by medical devices in the nursing setting can provide support for prioritization and increase the patient safety. However, the field of research lacks of knowledge when it comes to the patients' and nurses' experience of using PCA pumps with wireless communication system. Due to today's research field, further studies will be needed to investigate how documentation can be safeguarded and how accessible information regarding patients' need for pain relief can be linked to prescribed treatment. This may also lead to the development of nurses' way of work with patient-controlled and epidural pain relief in the postoperative pain management.

NCT ID: NCT03696095 Completed - Postoperative Pain Clinical Trials

Local Anesthetic Automated Intermittent Administration vs. Continuous Infusion Via Femoral Nerve Block.

Start date: April 16, 2018
Phase: Phase 4
Study type: Interventional

This study evaluates the impact of local anesthetic administration regiment through peri-neural femoral nerve catheter on pain and motor block frequency, after total knee arthroplasty.

NCT ID: NCT03695640 Recruiting - Postoperative Pain Clinical Trials

Effect of Magnesium Sulphate on Analgesia Following Knee Arthroplasty

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

This study is designed to investigate the effect of magnesium sulfate added to levobupivacaine in continuous femoral nerve block following total knee arthroplasty.

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.