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Postoperative Pain clinical trials

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NCT ID: NCT03112915 Recruiting - Postoperative Pain Clinical Trials

Comparison of the Quadratus Lumborum Block With the Transversus Abdominis Plan Block

Start date: April 20, 2017
Phase: N/A
Study type: Interventional

In this study, investigators aimed to compare the Quadratus Lumborum Block and the Transversus Abdominis Plan Block for postoperative pain control after laparoscopic cholecystectomy

NCT ID: NCT03107702 Enrolling by invitation - POSTOPERATIVE PAIN Clinical Trials

Melatonin Level and Postoperative Analgesia Consumption in Bariatric Surgery Patients.

Start date: March 29, 2017
Phase: N/A
Study type: Observational

Bariatric surgical procedures are associated with low short-term mortality and may be associated with long-term reductions in all-cause, cardiovascular, and cancer-related mortality. This surgeries are major surgeries include risk of mortality still. Melatonin is a hormone secreted from the pineal gland. Melatonin is an antioxidant, antinociceptive, hypnotic, anticonvulsant, neuroprotective, anxiolytic, sedative and analgesic. Melatonin is neurohormone with the profile of a novel hypnotic-anesthetic agent. The purpose of this study is to investigate the preoperative, perioperative and postoperative melatonin levels in bariatric surgery under general anesthesia and to investigate the relationship between melatonin level and analgesia requirement.

NCT ID: NCT03106818 Completed - Postoperative Pain Clinical Trials

Postoperative Pain Alleviation in Open Heart Surgery

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

Effective pain relief after cardiac surgery has assumed importance with the introduction of fast track discharge protocols that requires early weaning from mechanical ventilation. Inadequate pain control reduces the capacity to cough, mobility, increases the frequency of atelectasis, and prolongs recovery. Infiltration of local anesthetics near the surgical wound has shown to improve early postoperative pain in various surgical procedures. Magnesium is the fourth most plentiful cation in our body. It has antinociceptive effects in animal and human models of pain.

NCT ID: NCT03105518 Active, not recruiting - Postoperative Pain Clinical Trials

Predictors of Postoperative Pain Following Oocyte Retrieval for Assisted Reproduction

Start date: March 1, 2011
Phase: Phase 4
Study type: Interventional

The central objective of this study will be to evaluate the relationship between estrogen levels and the pain following oocyte retrieval in women undergoing in vitro fertilization.

NCT ID: NCT03102515 Completed - Postoperative Pain Clinical Trials

Transversus Abdominis Plane Block vs Continuous Infiltration Wound Catheter for Analgesia After Caesarean Section

TAP-CAT
Start date: May 29, 2016
Phase: Phase 4
Study type: Interventional

Analgesia following surgery associates different intra-venous or oral analgesic drugs and sometimes opioids. To reduce opioid consumption, loco-regional anaesthesia might be administered as a complement. In the specific context of caesarean sections, pain control is mandatory to enable the mother to take care of her offspring and shorten their hospital stay. This intervention is mainly performed under neuraxial anaesthesia (spinal or epidural), enabling the injection of morphine in the subdural or epidural space, as part of a multimodal analgesia regimen. Studies have evaluated continuous wound infiltration catheters (CIC) and ultrasound-guided (UGD) transabdominis plane (TAP) block, and both techniques and both techniques reduce postoperative morphine consumption. Recent studies have compared the two techniques and found conflicting results. Furthermore, they did not consider caesarean section performed under epidural analgesia, with a different neuraxial injection site, neither did they compared pain after postoperative day 2. Consequently, the aim of this study was to compare resting and standing pain up to postoperative day 3 after caesarean section performed under spinal or epidural anaesthesia and receiving either USG-TAP block or CIC. Baseline hypothesis was that the continuous infiltration provided a better analgesia at day 2.

NCT ID: NCT03100669 Completed - Postoperative Pain Clinical Trials

Implementing a Postoperative MIRP (Minimally Invasive Repair of Pectus) Program Via Tele-monitoring

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

MIRP (Minimally Invasive Repair of Pectus) as surgical correction of pectus excavatum or carinatum is performed to achieve physiological, cosmetic, and psychological benefits for the patient. Surgery is often associated with severe postoperative pain. In this study the researchers want to registrate pain, sleep, nausea/vomiting, and daily activities in short and long term follow up.

NCT ID: NCT03098667 Completed - Postoperative Pain Clinical Trials

Laryngeal Mask Airway (LMA) Protector for Minimally Invasive Thyroidectomy

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

The patients will be allocated to 2 groups: the LMA group and the endotracheal tube (ET) group. Airway management will be done with the LMA Protector for the patients of the LMA group and with the classic endotracheal tube for the patients of the ET group. The main purpose of the study is to determine if the application of the LMA Protector causes less laryngopharyngeal symptoms than the endotracheal tube after minimally invasive thyroidectomy. The secondary purpose is to confirm that the LMA Protector is a safe alternative airway management device for minimally invasive thyroidectomy.

NCT ID: NCT03084601 Completed - Postoperative Pain Clinical Trials

Evaluation of Postoperative Pain After Using 3MIX-TATIN Versus Calcium Hydroxide Iodoform Paste In Necrotic Primary Molars Treated by Lesion Sterilization and Tissue Repair Therapy

3-mixtatin
Start date: March 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of the current study is to compare a newly introduced material which is a combination of triple mix antibiotics paste and anti-hyperlipidemia drug simvastatin, the new material is named 3MIX-TATIN & will be compared to triple antibiotic paste for management of necrotic primary molars by using lesion sterilization and tissue repair LSTR technique.

NCT ID: NCT03079830 Completed - Clinical trials for Aortic Valve Surgery

Postoperative Pain Management After Minimally Invasive Aortic Valve Surgery

PPMAMIAVS
Start date: October 2016
Phase: N/A
Study type: Interventional

The study evaluates the efficacy of local anesthestic application through the catheter in the surgical wound for the postoperative pain relief after minimally invasive aortic valve surgery. The patients will be enrolled in two different groups according to the protocol of the local anesthetic and saline administration: 1. group: continous infusion of the local anesthetic plus bolus on demand 2. group: continous infusion of saline plus bolus on demand For all patients metamizol every 12 hours plus bolous of piritramid on demand.

NCT ID: NCT03074097 Completed - Postoperative Pain Clinical Trials

Rectus Sheath Block: Postoperative Analgesia and Proinflammatory Cytokines

Start date: March 5, 2015
Phase: Phase 2
Study type: Interventional

Good quality of postoperative analgesia would lead to attenuate or prevent the adverse effects on the common functions of the immune system. We compared the effect of epidural analgesia versus rectus sheath block on postoperative pain and proinflammatory cytokines following malignant urological surgery.