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Pain, Postoperative clinical trials

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NCT ID: NCT03397069 Completed - Postoperative Pain Clinical Trials

Midazolam Additive to Local Anesthetic in Peribulbar Block

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

Regional eye blocks are usually preferred for ophthalmic procedures. Peribulbar block (PBB) is a safe alternative for patients undergoing cataract surgery. Many studies tried to solve this issue by means of prolonging the duration of action of the local anesthetics used. Several drugs were tried as adjuncts to local anesthetics, and their effects have been studied. Midazolam added to the list of adjuvant used in the subarachnoid or epidural block can produce analgesia, probably mediated by the benzodiazepine-Gamma Amino-Butyric Acid(GABA) receptor complex. The investigators hypothesized that the addition of midazolam to lidocaine will improve the quality of the peribulbar block; fasten the onset and prolonging its anesthetic and analgesic duration.

NCT ID: NCT03396991 Completed - Pain, Postoperative Clinical Trials

Comparative Evaluation of Two Different Post-Operative Analgesia After Hallux Valgus Correction

Start date: July 1, 2017
Phase:
Study type: Observational [Patient Registry]

Background: Recent studies showed the efficiency of several techniques of anesthesia in foot surgery. The new mini-invasive surgical approaches should require less analgesia and rapid motor recovery after surgery. The aim of this study was the evaluation of two different techniques on postoperative analgesia and motor recovery after hallux valgus correction in one-day surgery patients.

NCT ID: NCT03395912 Completed - Cesarean Section Clinical Trials

Wound Infiltration With Bupivacaine/Adrenalin During Cesarean Section and Postoperative Pain.

Start date: January 25, 2018
Phase: N/A
Study type: Interventional

Thus study evaluates the advantage of infiltration of the surgical wound by local anesthetics in cesarean section on post operative pain relief. In the study group before closing the skin, both sides of the incision (top and bottom) will be infiltrated by 30 ml of 0.25% BUPIVACAINE and ADRENALIN at 1: 200,000 concentration and then closing the skin. In the control group, the skin will be closed without infiltration. Our hypothesis is that subcutaneous infiltration of the surgical wound by BUPIVACAINE + ADRENALIN at the end of cesarean section will reduce the intensity of post operative pain.

NCT ID: NCT03393949 Completed - Postoperative Pain Clinical Trials

Effects of Methylprednisolone on Immunological Function and Postoperative Pain

Start date: July 1, 2015
Phase: Phase 4
Study type: Interventional

Surgical trauma is characterized by a tightly integrated sequence of neurohumoral and immunological processes. When this is marked, it can manifest as a clinical entity called the systemic inflammatory response syndrome. Previous studies reported that inflammatory milieu in the postoperative period can be a harmful and potentially modifiable condition that may affect postoperative recovery, which includes the level of pain, fatigue, dizziness, nausea and vomiting (PONV), muscle weakness, and sleep quality and then increases the need for hospitalization. The effect of postoperative inflammation-related immune suppression such as the T-cell exhaustion and lymphocyte anergy may render the patient vulnerable to both infection and the recurrence of malignancy on postoperative infection risk and malignancy recurrence are currently subjects of intense speculation and investigation. Glucocorticoids are well known for their analgesic, anti-inflammatory, immunosuppressive agents and antiemetic effects. Though previous studies' results on postoperative outcome have been positive and in favor of glucocorticoid use, with postoperative nausea and vomiting and pain outcome parameters most significantly improved. However, high-dose methylprednisolone treatment could result in decreases T-cells postoperatively. Based on these consideration, the aim of our study was to assess the effect of a single low-dose preoperative methylprednisolone (MP) 1 mg/Kg i.v. on postoperative pain and immune functions in patients undergoing video-assisted thoracoscopic surgery (VATS) under general anesthesia.

NCT ID: NCT03393702 Completed - Pain, Postoperative Clinical Trials

Pain Control in Children and Adolescent After Thoracic Surgery: The Effect of Gabapentin

Start date: May 9, 2017
Phase: Phase 4
Study type: Interventional

The study is performed in patients aged 5-18 years after thoracic surgery. The primary aim of this trial is to determine whether the use of gabapentin as a component of multimodal analgesic regiments reduces pain scores following thoracic surgery in pediatric patients. The secondary objective of the trial are to evaluate whether the use of gabapentin reduces postoperative anxiety scores and consumption of ropivacaine with fentanyl, decreases side-effects, and improves patient satisfaction.

NCT ID: NCT03393572 Completed - Anesthesia Clinical Trials

Intraperitoneal Bupivacaine With Magnesium or Nalbuphine for Postoperative Pain Control in Laparoscopic Hysterectomy

Start date: January 3, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare between the addition of Mg sulphate or Nalbuphine to intraperitoneal bupivacaine installation in laparoscopic hysterectomy for postoperative pain control and their relative adverse effects.

NCT ID: NCT03393403 Recruiting - Gastric Cancer Clinical Trials

Comparison of the Effect of Intravenous and Perineural Dexmedetomidine in Gastric Cancer Surgery

Start date: December 23, 2017
Phase: N/A
Study type: Interventional

Using random case assignment to investigate the analgesic and sedative effect of intravenous dexmedetomidine and dexmedetomidine as a local anesthetic adjuvant in ultrasound-guided subcostal TAP block in gastric cancer patient undergoing gastrectomy or partial gastrectomy.

NCT ID: NCT03391570 Recruiting - Clinical trials for Female Genital Disease

Comparing Postoperative Pain Following COX-2 and Prostanoids Expression

COX2RCT
Start date: October 17, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to compare postoperative pain following COX-2 and prostanoids expression in women who underwent laparoscopic surgery for female genital disease in order to evaluate the effect of COX-2 on local inflammation, COX-2 and prostanoids expression followed by exposure time to carbon dioxide(CO2) gas, and degree of postoperative pain.

NCT ID: NCT03391284 Completed - Post-operative Pain Clinical Trials

Oral vs Intravenous Acetominophen for Postoperative Pain in Minimally Invasive Gynecologic Surgery

Start date: February 2016
Phase: N/A
Study type: Interventional

Hypothesis: Postoperative pain will be equivalent in patients receiving preemptive oral acetaminophen as compared to patients receiving preemptive intravenous acetaminophen following minimally invasive benign gynecologic surgery. Primary outcome: • Difference in postoperative pain comparing preemptive use of PO versus IV acetaminophen o Mean Visual analog Scale (VAS) scores will be compared between the intervention group (PO acetaminophen) and the control group (IV acetaminophen). Secondary outcomes: - Difference in postoperative analgesic use between groups o Narcotics, NSAIDs - Difference in postoperative N/V between groups o Patient rated measure - none, mild, moderate, severe - Cost comparison between drugs

NCT ID: NCT03391167 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Bilateral Erector Spinae Plane Block in Laparoscopic Cholecystectomy

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

This study will define the postoperative analgesic effect of ESP block via amount of patient-controlled analgesia (PCA) and postoperative analgesic consumption (such as routinely and rescue analgesics) and compare the control group in patients having laparoscopic Cholecystectomy .