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Pain, Postoperative clinical trials

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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: 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: 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: 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.