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Postoperative Vomiting clinical trials

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NCT ID: NCT03712891 Active, not recruiting - Clinical trials for Patient Satisfaction

Evaluation of Providing Coffee to Patients Postoperatively to Decrease Length of Stay in the PACU

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

The purpose of the study is to determine if providing coffee to patients who self-identify as coffee drinkers postoperatively will decrease the length of stay in the post-anesthesia care unit (PACU).

NCT ID: NCT03142464 Completed - Clinical trials for Postoperative Nausea

Intravenous Fluids After Laparoscopic Cholecystectomy

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

Perioperative intravenous fluid (IV) administration has been the standard procedure since 1832 and, is a widely used practice sometimes under inadequate criteria. The present work aims at verifying the clinical need that justifies the common IV fluid prescription on the postoperative (PO) period in patients undergoing videolaparoscopic cholecystectomy (CVL) elective.

NCT ID: NCT03141645 Completed - Clinical trials for Postoperative Nausea and Vomiting

Comparison of IV Fluid Loading and Ondansetron in Reduction of PONV After LC

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

This study is designed to examine the incidence of postoperative nausea and vomiting during 24 hours after elective laparoscopic cholecystectomy in patients receiving preoperative intravenous fluid loading (group F), ondansetron (group O) and receiving neither fluid nor ondansetron or control group (group C).

NCT ID: NCT02765750 Terminated - Postoperative Pain Clinical Trials

Postoperative Outcomes After Positive Intraoperative Messages

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

The patients scheduled for laparoscopic cholecystectomy will be allocated to 3 groups. Group A and B patients will listen to a positive message under general anesthesia. Group C patients will not listen to the message. The postoperative pain, analgesic consumption and frequency of nausea, vomiting and emergence agitation episodes will be documented and compared between the 3 groups.

NCT ID: NCT02744495 Completed - Clinical trials for Postoperative Nausea

Prophylaxis of Postoperative Nausea and Vomiting After Cardiac Surgery

PONVACS
Start date: February 2016
Phase: Phase 3
Study type: Interventional

To investigate the role of postoperative nausea and vomiting risk factors assessment after cardiac surgery. We designed a randomized controlled study comparing standard care (no risk factor assessment and no intervention) with prophylaxis of postoperative nausea and vomiting after cardiac surgery in high risk patients. Prophylaxis of postoperative nausea and vomiting by betamethasone (4mg) and/or droperidol (0.625mg) immediately after cardiac surgery, depending on risk factors (if risk score is over 2) in the intervention arm.

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: NCT02177201 Completed - Clinical trials for Postoperative Vomiting

Effect of Intraoperative Crystalloid Volume on Postoperative Vomiting

EICVPV
Start date: August 2013
Phase: N/A
Study type: Interventional

Postoperative nausea and vomiting is very common in children undergone tonsillectomy and/or adenoidectomy. The purpose of this clinical trial is to evaluate the antiemetic effect of super-hydration with 0.9% saline in children undergoing specifically elective otorhinolaryngological surgery. Fluid intake reduces vomiting as seen following extended period of fasting that interrupts the perfusion in gut. Based on this knowledge, we hypothesized that administration of supplemental fluid would reduce the incidence of postoperative vomiting.

NCT ID: NCT01912807 Completed - Clinical trials for Postoperative Vomiting

Postoperative Vomiting in Children - Is Dextrose an Effective Prophylactic Anti-emetic?

DEXPO
Start date: December 2013
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the efficacy of intraoperative intravenous dextrose in preventing POV in pediatric population undergoing dental day surgery. Post-operative vomiting (POV) in children is a frequent complication. Studies using intravenous (IV) fluids containing dextrose in the perioperative period have shown improvement of POV in adults. Similar studies have not been done in children. Knowing that Intravenous (IV) fluids containing dextrose are safe and commonly used in the paediatric population, this intervention could potentially reduce the amount of rescue antiemetic medications and improve recovery in same-day surgery paediatric patients.

NCT ID: NCT01798316 Terminated - Postoperative Pain Clinical Trials

IV Acetaminophen for Postoperative Analgesia

Start date: March 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the use of IV acetaminophen for postoperative pain management after laparoscopic cholecystectomy to determine if its use to supplement standard of care pain management decreases the incidence of post-operative nausea and vomiting.

NCT ID: NCT01739985 Completed - Clinical trials for Postoperative Vomiting

Postoperative Vomiting in Children: Comparison Tri - Versus bi -Prophylaxis

VPOP2
Start date: December 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the benefit of addition of droperidol to prophylaxis with ondansetron and dexamethasone in children with high risk of postoperative vomiting (POV). In adults some authors showed that the effectiveness of prophylaxis is correlated to the number of molecules or specific procedures used.