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Pain, Postoperative clinical trials

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NCT ID: NCT02549105 Recruiting - Post Operative Pain Clinical Trials

Lidocaine-Prilocaine Cream (EMLA) Topical Application Versus Wound Infiltration With Lidocaine After Cesarean Section

Start date: October 2014
Phase: Phase 4
Study type: Interventional

A Comparison Between Lidocaine-Prilocaine Cream (EMLA) Application And wound Infiltration with Lidocaine For Post Caesarean Section Pain Relief : A Randomized Controlled Trial.

NCT ID: NCT02548104 Recruiting - Pain, Postoperative Clinical Trials

Analgesic Efficacy of Anterior Femoral, Genicular and Adductor Canal Nerve Block

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

Recently, more distal approach to femoral nerve branches (saphenous) in the adductor canal in the medial compartment of the thigh have shown to provide comparable anesthesia and analgesia without quadriceps muscle weakness than traditional femoral nerve blocks (FNB) after total knee arthroplasty (TKA). Adductor canal block (ACB) has the unique advantage of providing localized analgesia to the peripatellar and intra-articular aspects of the knee joint without reducing the patient's ability to perform a straight leg raise. However, it does not adequately address the incisional pain component on the anterior surface of the knee innervated by anterior femoral cutaneous nerve. This pain may be improved by addition of the anterior femoral block (AFB). Additionally, the ACB does not provide analgesia to the posterior aspect of the knee, which is commonly moderate to severe after surgery. This pain may be decreased by addition of the genicular block, also known as the iPACK block (interspace between the popliteal artery and the capsule of the knee). There is no study that has evaluated the potentially analgesic benefits of the AFB or the iPACK block combined with ACB after TKA. Therefore, the investigators designed this randomized, prospective, and double-blinded study to assess our hypothesis that the addition of the AFB and/or iPACK block to the ACB will improve analgesic effects, decrease pain scores, deceased opioid requirement, and as well as facilitate early recovery and improve patient satisfaction with pain management in patient after TKA.

NCT ID: NCT02523846 Recruiting - Post-operative Pain Clinical Trials

Patient Re-education vs. Background Morphine to IV-PCA in Patient With Unsatisfactory Analgesia Post Laparotomy

Start date: August 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to improve IV-Patient Controlled Analgesia (IV-PCA) technique for postoperative analgesia. Investigators are comparing between patient re-education and the background morphine infusion among patients who fail to achieve satisfactory analgesia using IV-PCA Morphine after laparotomy.

NCT ID: NCT02513979 Recruiting - Hypertension Clinical Trials

Postoperative Pain and Angiotensin II Receptor Antagonists

PP&ARA
Start date: August 2015
Phase: Phase 4
Study type: Interventional

An angiotensin II type 2 receptor (AT2R) antagonist has been assessed for its efficacy in neuropathic pain with promising results. A considerable number of patients undergoing surgery under general anesthesia are hypertensive and receive drugs to control high blood pressure, including angiotensin II receptor antagonists. These drugs may attenuate the acute and/or chronic postoperative pain or decrease the analgesic requirements after surgery. The aim of the present study is to assess the early postoperative pain and analgesic requirements in patients treated with antagonists of the angiotensin II receptors for at least three months before surgery compared to normotensive patients.

NCT ID: NCT02495220 Recruiting - Postoperative Pain Clinical Trials

Efficacy of Dexmedetomidine for Postoperative Analgesia in Infantile Cataract Surgery

Start date: July 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the present study was to evaluate the efficacy and safety of subtenon block (SB)anesthesia with dexmedetomidine in combination with bupivacaine versus intravenous dexmedetomidine for postoperative analgesia and emesis control in infants undergoing cataract surgery.

NCT ID: NCT02487355 Recruiting - Pain, Postoperative Clinical Trials

Pediatric Caudal Dexmedetomidine Enhances Postoperative Analgesia of Magnesium Sulphate in Lower Abdominal Surgeries

JASayed
Start date: May 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The study will conduct to compare the efficacy of Magnesium sulphate & dexmedetomidine used as adjuvants to bupivacaine in caudal block to provide intra-operative anesthesia as well as post -operative analgesia in pediatric patients.

NCT ID: NCT02483689 Recruiting - Post Operative Pain Clinical Trials

Evaluation of Local Anesthetic at Incision Site

Start date: August 2015
Phase: N/A
Study type: Interventional

Patient will have usual appendectomy surgery with an injection of local or saline at incision site either before or after the incision at random. The clinical hypothesis of this trial is that pediatric patients who undergo a local anesthetic pre-incisional and/or post-incisional will reduce the amount of postoperative pain and therefore reduce the amount of analgesics required to keep the patient satisfied. Primary: To determine if local anesthetic reduces postoperative pain. Secondary: To assess the timing of local anesthetic injection affects postoperative pain.

NCT ID: NCT02483338 Recruiting - Postoperative Pain Clinical Trials

FASS (Facial Action Summary Score) Scale to Differentiate the Pain of Postoperative Anxiety in Children Under 7 Years

FASS
Start date: July 2011
Phase: N/A
Study type: Interventional

This study aims to evaluate the psychometric validity of FASS (Facial Summary Score Scale) to assess postoperative children pain.

NCT ID: NCT02476370 Recruiting - Anxiety Clinical Trials

Effects of Preoperative Relaxation and Intensified Surgery Education in Patients Undergoing Herniotomy

MBM_Hernio
Start date: June 2015
Phase: N/A
Study type: Interventional

This study aims to test the effects of a Preoperative Relaxation intervention and an Intensified Surgery Patient Education on pre- and postoperative wellbeing and health in Patients Undergoing Herniotomy.

NCT ID: NCT02456116 Recruiting - Pain, Postoperative Clinical Trials

Efficiency Study About the Effect of Acupuncture on Postoperative Pain After Total Knee Arthroplasty

APOPKA
Start date: September 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the use of needle acupuncture in comparison to a conventional postoperative pain management in terms of reducing pain and pain medication use in an interdisciplinary setting in a controlled, randomized study design after implantation of total knee arthroplasty .