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Pain, Postoperative clinical trials

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NCT ID: NCT03771755 Not yet recruiting - Postoperative Pain Clinical Trials

Ibuprofen IV vs Acetaminophen IV for the Treatment of Pain Following Orthopaedic Low Extremity Surgery

Start date: January 2019
Phase: N/A
Study type: Interventional

This study aims to evaluate the efficacy of IV Ibuprofen versus IV Acetaminophen in the reduction of pain following orthopedic low extremity procedures

NCT ID: NCT03771339 Not yet recruiting - Postoperative Pain Clinical Trials

Comparison of Quadratus Lumborum Block and Epidural Analgesia Following Kidney Transplant Surgery

Start date: December 10, 2018
Phase: N/A
Study type: Interventional

Quadratus lumborum block as an alternative for postoperative analgesia compared with epidural block

NCT ID: NCT03770013 Not yet recruiting - Postoperative Pain Clinical Trials

Dexmedetomidine Versus Clonidine for Transversus Abdominis Plane Block in Patients Undergoing Elective Caesarean Section

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Aim to study the efficacy of co-administered Dexmedetomidine Or Clonidine with Bupivacaine and that of bupivacaine 0.25% alone for Transversus Abdominis Plane (TAP) Block for Postoperative Analgesia in Patients Undergoing Elective Caesarean Section. - Group 1: bupivacaine 0.25% + Dexmedetomidine 0.5 mcg/kg (a total volume of 40 ml (20 ml each side) was used for the TAP block.) - Group 2: 20 ml bupivacaine+1ug/kg clonidine bilaterally (a total volume of 40 ml (20 ml each side) was used for the TAP - Group3: bupivacaine 0.25% + placebo (a total volume of 40 ml (20 ml each side) was used for the TAP A prospective Randomized Interventional double-blind study.

NCT ID: NCT03769818 Not yet recruiting - Postoperative Pain Clinical Trials

Role of Dexamethasone for Erector Spinae Plane Block in Patients Undergoing Total Abdominal Hysterectomy

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The aim to study the efficacy of bupivacaine 0.25% with dexamethasone and that of bupivacaine 0.25% alone for erector spinae plane block for postoperative analgesia in patients undergoing total abdominal hysterectomy Group 1: bupivacaine 0.25% + dexamethasone 8 mg - Group 2: bupivacaine 0.25% - Group3: control group A prospective Randomized Interventional double-blind study.

NCT ID: NCT03768440 Not yet recruiting - Pain, Postoperative Clinical Trials

Continuous Erector Spinae Block Versus Continuous Paravertebral Block

Start date: January 2019
Phase: Phase 3
Study type: Interventional

Overall Aim: To evaluate the efficacy of continuous erector spinae block (ESB) versus continuous paravertebral block (PVB) for postoperative analgesia in children and adolescents undergoing surgical procedures via unilateral thoracotomy. Hypothesis: The investigators hypothesize that ESP block efficacy is not inferior to that of PVB with respect to pain control and consumed opiate equivalents at 24 hours postoperatively.

NCT ID: NCT03768193 Completed - Pain, Postoperative Clinical Trials

Deep Serratus Anterior Plane Block vs Surgically-placed Paravertebral Block for VATS Surgery

SAPB
Start date: October 4, 2017
Phase: N/A
Study type: Interventional

Thoracic surgery, and surgery involving the chest wall in general, is associated with poorly controlled acute pain, which may result in delayed functional recovery, and may progress to chronic pain. Multimodal opioid-sparing analgesia regimens are a key component of the thoracic surgery enhanced recovery pathway, the aim of which is to improve outcomes in patients undergoing both minimally invasive and open thoracic surgical procedures. Novel interfascial plane blocks are emerging as feasible alternatives to central neuraxial analgesia techniques in a variety of clinical settings. The aim of this study is to show non-inferiority of serratus anterior blockade compared with surgically placed paravertebral blocks in the management of perioperative acute pain in patients undergoing VATS procedures.

NCT ID: NCT03768102 Not yet recruiting - Postoperative Pain Clinical Trials

Comparison of Verbal Rating Scale and Numerical Rating Scale in Post Anesthesia Care Unit

Start date: December 2018
Phase:
Study type: Observational

In the postanesthetic care unit(PACU), patients who are recovering from anesthesia are not easy to communicate with. Accordingly, accurate evaluation of acute surgical pain is difficult for PACU patients in spite of severe postoperative pain. Therefore, pain evaluation is clinically important and challenging in PACU. The pain evaluation tool should be simple and easy to understand for accurate assessment. Among the most commonly used pain assessment methods are numerical rating scale(NRS), visual analogue scale(VAS) and verbal rating scale(VRS). These three methods have proved valid for clinical situations in many studies. VRS appears to be easier to understand than the other two methods for patients in PACU. The purpose of this study is to compare NRS and VRS in PACU patients.

NCT ID: NCT03767816 Not yet recruiting - Clinical trials for Visceral Pain, Postoperative

The Visceral Analgesic Effect of Erector Spinae Plane Block in Laparoscopic Cholecystectomy

Start date: December 7, 2018
Phase: N/A
Study type: Interventional

The purpose of this study was to investigate the effectiveness of erector spinae plane block on postoperative visceral pain in laparoscopic cholecystectomy (LLC). Given that rectus sheath block may provide sufficient somatic pain block, investigators aimed to investigate whether erector spinae block is effective in visceral pain block. After induction of general anesthesia, group of patient is decided randomly. In Group R, rectus sheath block is performed with 0.2% Ropivacaine 30ml before the operation. In Group RE, rectus sheath block and erector spinae plane block are performed with 0.2% ropivacaine 70ml before the operation. NRS score measurement and comparison of the rescue analgesic dose used at 0, 0.5, 1, 2,6, 12, 18, and 24 hours after arrival at the recovery room were collected

NCT ID: NCT03765827 Not yet recruiting - Postoperative Pain Clinical Trials

Vitamin E on Staple Line and Anastomoses of Roux-en-Y Gastric Bypass

Start date: December 5, 2018
Phase: Phase 3
Study type: Interventional

Patients will be randomized into 2 groups: - Vit E group: Vitamin E ointment will be applied over staple lines and anastomoses - Control group: Vitamin E will not be applied Postoperative pain will be assessed 24 hours after surgery.

NCT ID: NCT03765723 Not yet recruiting - Anesthesia Clinical Trials

Prediction Model of Acute Postoperative Pain in Bilateral Total Knee Replacement Arthroplasty Patient

Start date: January 1, 2019
Phase:
Study type: Observational

This study aims to predict risk factors of acute postoperative pain of the patients undergoing Total Knee Replacement Arthroplasty(TKRA).