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Prophylactic Antiemetic Efficacy of Palonosetron Versus Ondansetron for the Prophylaxis of Postoperative Nausea and Vomiting (PONV) in Women Over 60 Years Undergoing Laparoscopic Cholecystectomy

Primary Purpose

Postoperative Nausea and Vomiting

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Ondansetron
Palonosetron
Sponsored by
Hospital Federal de Bonsucesso
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postoperative Nausea and Vomiting focused on measuring C23.888.821.712.700

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Will be selected patients aged over 60 years, ASA 1-3 that are candidates for laparoscopic cholecystectomy

Exclusion Criteria:

  • Participation in another study last month.
  • Body mass index> 35.
  • The occurrence of episodes of nausea or vomiting in the last 24 h prior to surgery.
  • Use of corticosteroids.
  • Smoking.
  • Alcoholism.
  • Use of psychoactive drugs or any other drug with antiemetic effect.
  • Known hypersensitivity to any study medication
  • Severe diseases in organs such as kidney, liver, lung, heart, brain and bone marrow.
  • Conversion laparoscopic cholecystectomy for conventional cholecystectomy.

Sites / Locations

  • Hospital Federal de Bonsucesso

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Palonosetron

Ondansetron

Arm Description

Palonosetron (iv) one minute before anesthesic induction.

ondansetron (iv) one minute before anesthesic induction and ondansetron regular three times a day for two days after the surgery.

Outcomes

Primary Outcome Measures

Frequency and intensity of individual episodes of PONV.

Secondary Outcome Measures

Intensity of nausea
Evaluate nausea intensity in numeric scale (0-10) during clinical visit
Need of medication for antiemetic rescue
Assess the need of medication for antiemetic rescue during the 48 h after surgery
Number of complete responders to medication
Determine the number of complete responders to medications (no emetic episode or rescue medication during the 48 hours after surgery)
Degree of satisfaction with antiemetic therapy
Know the degree of satisfaction with antiemetic therapy, through the 5-point rating scale (very dissatisfied, dissatisfied, neutral, satisfied or very satisfied)
Cost of antiemetic medication
total cost of antiemetic therapy (including 5HT3 antagonist and rescue medication), based on the table "Brasíndice".
Frequency and intensity of adverse effects
Determine the frequency and intensity of adverse effects by means of numerical scale(0-10) (headache, dizziness, drowsiness and others)
Frequency of polymorphism of 5HT3a receptors and 5HT3b
To assess the frequency of polymorphism and 5HT3b 5HT3a receptors and their correlation with the frequency and intensity of antiemetic effect and adverse effects.

Full Information

First Posted
August 25, 2015
Last Updated
August 8, 2017
Sponsor
Hospital Federal de Bonsucesso
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1. Study Identification

Unique Protocol Identification Number
NCT02541019
Brief Title
Prophylactic Antiemetic Efficacy of Palonosetron Versus Ondansetron for the Prophylaxis of Postoperative Nausea and Vomiting (PONV) in Women Over 60 Years Undergoing Laparoscopic Cholecystectomy
Official Title
Prophylactic Antiemetic Efficacy of Palonosetron Versus Ondansetron for the Prophylaxis of Postoperative Nausea and Vomiting (PONV) in Women Over 60 Years Undergoing Laparoscopic Cholecystectomy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
January 1, 2017 (Actual)
Study Completion Date
July 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Federal de Bonsucesso

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite the development of new drugs, nausea and vomiting after surgery (PONV) are still frequent. Antagonists 5HT3 receptors, such as ondansetron and palanosetron, are among the main characterized prophylactic agents in patients at high risk, however there are few studies comparing the efficacy of these drugs and no study that addresses women aged over 60 years. In this prospective, randomized, double-blind study, 80 women nonsmokers, undergoing laparoscopic cholecystectomy will be divided into two groups, receiving during anesthetic induction intravenous ondansetron 4 mg (n = 40) or palonosetron 75 mcg (n = 40) prophylaxis of PONV.
Detailed Description
Clinical, prospective, randomized double-blind trial will be conducted at the Federal Hospital Bonsucesso (HFB), Rio de Janeiro, Brazil. Eighty female patients, olther than 60 years, ASA I to III, undergoing laparoscopic cholecystectomy will be studied. They will be randomized into two groups of 40. One group will receive Palonosetron 75 mcg (Group P) and the other will receive Ondansetron 4mg (Group O). Patients will not receive premedication. Will be monitored in the operating room with non-invasive blood pressure, cardioscopy, pulse oximetry, capnography and bispectral index (BIS). After cannulation of peripheral vein, 10 ml of blood will be collected for further analysis. They will be given one minute before induction of anesthesia, intravenous (IV) bolus preparations of the studied antiemetics. Patients will be pre-oxygenated with oxygen at 100% for 5 minutes and the anesthetic induction is performed with intravenous administration of fentanyl 3 mcg / kg; Lidocaine 1.5 mg / kg and propofol 2 mg / kg. Tracheal intubation will be facilitated after 3 minutes of administration of Rocuronium 0.6 mg / kg EV .Maintenance of anesthesia will be with Sevoflurane 2 L / min in 50% oxygen / air, with its concentration adjusted to maintain BIS between 40-60. Remifentanil 0.05 mcg / kg / min to 0.2 mcg / kg / min IV can be administered intraoperatively if the heart rate or blood pressure to rise more than 20% of values baseline. Additional doses of rocuronium may also be administered as needed. Patients will receive paracoxibe 40 mg,dipirone 50 mg / kg and 50 mg of ranitidine IV after tracheal intubation and have the surgical wound infiltration with 20 mL of ropivacaine 0.5%, before the sutures. Neuromuscular blockade reversed with neostigmine 0.04 mg / kg and atropine 0.02 mg / kg IV at the end of surgery. Will be limited to insufflation of the pneumoperitoneum to abdominal pressure of 15 mmHg. A non-participating physician will be aware of the research on which antiemetic was given and be responsible for postoperative prescription of patients. The researchers did not have access to prescription and medical records within 48 hours after surgery. Both groups will recive metoclopramide 10 mg (EV) as rescue medication for PONV, and the Group O will continue with prescription ondansetron 4 mg (EV) regular 8 / 8h, in the following 48 h after surgery. Patients will receive clinical visit by the research team 2, 6, 24 and 48 h after the end of surgery and will be questioned about the frequency and intensity of PONV, as well as other side effects. Finished the last evaluation, researchers will review the prescription and will note the use of opioids (type, dose, route of administration), use of rescue medication, total cost of antiemetic therapy (including 5HT3 antagonist and rescue medication), based on "Brasíndice" table. All patients have their blood samples analyzed in the clinical research laboratory of the Universidade Federal Fluminense, for concurrent research of prevalence of polymorphisms of 5HT3 receptors and their correlation with the antiemetic effect. DNA will be extracted from blood samples using a kit to genomic DNA purification. Polymerase chain reaction test for real time will be applied below for analysis of single nucleotide polymorphisms of. The reactions are prepared with Genotyping according to the manufacturer's instructions and performed on a sequence detection system using standard thermal cycling conditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postoperative Nausea and Vomiting
Keywords
C23.888.821.712.700

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Palonosetron
Arm Type
Experimental
Arm Description
Palonosetron (iv) one minute before anesthesic induction.
Arm Title
Ondansetron
Arm Type
Experimental
Arm Description
ondansetron (iv) one minute before anesthesic induction and ondansetron regular three times a day for two days after the surgery.
Intervention Type
Drug
Intervention Name(s)
Ondansetron
Intervention Description
4 mg IV, one minute before the anesthesia induction and 4 mg IV three times a day during two days after the surgery.
Intervention Type
Drug
Intervention Name(s)
Palonosetron
Intervention Description
75 mcg IV, one minute before the anesthesia induction.
Primary Outcome Measure Information:
Title
Frequency and intensity of individual episodes of PONV.
Time Frame
48 h after surgery
Secondary Outcome Measure Information:
Title
Intensity of nausea
Description
Evaluate nausea intensity in numeric scale (0-10) during clinical visit
Time Frame
during clinical visit 2, 6, 24 and 48 h postoperatively
Title
Need of medication for antiemetic rescue
Description
Assess the need of medication for antiemetic rescue during the 48 h after surgery
Time Frame
during the 48 h after surgery
Title
Number of complete responders to medication
Description
Determine the number of complete responders to medications (no emetic episode or rescue medication during the 48 hours after surgery)
Time Frame
during the 48 h after surgery
Title
Degree of satisfaction with antiemetic therapy
Description
Know the degree of satisfaction with antiemetic therapy, through the 5-point rating scale (very dissatisfied, dissatisfied, neutral, satisfied or very satisfied)
Time Frame
during the 48 h after surgery
Title
Cost of antiemetic medication
Description
total cost of antiemetic therapy (including 5HT3 antagonist and rescue medication), based on the table "Brasíndice".
Time Frame
during the 48 h after surgery
Title
Frequency and intensity of adverse effects
Description
Determine the frequency and intensity of adverse effects by means of numerical scale(0-10) (headache, dizziness, drowsiness and others)
Time Frame
during the 48 h after surgery
Title
Frequency of polymorphism of 5HT3a receptors and 5HT3b
Description
To assess the frequency of polymorphism and 5HT3b 5HT3a receptors and their correlation with the frequency and intensity of antiemetic effect and adverse effects.
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 48 h

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Will be selected patients aged over 60 years, ASA 1-3 that are candidates for laparoscopic cholecystectomy Exclusion Criteria: Participation in another study last month. Body mass index> 35. The occurrence of episodes of nausea or vomiting in the last 24 h prior to surgery. Use of corticosteroids. Smoking. Alcoholism. Use of psychoactive drugs or any other drug with antiemetic effect. Known hypersensitivity to any study medication Severe diseases in organs such as kidney, liver, lung, heart, brain and bone marrow. Conversion laparoscopic cholecystectomy for conventional cholecystectomy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ismar L Cavalcanti, PhD
Organizational Affiliation
UFF
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Federal de Bonsucesso
City
Rio de Janeiro
ZIP/Postal Code
21041-030
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
24495419
Citation
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Results Reference
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Citation
Silva AC, O'Ryan F, Poor DB. Postoperative nausea and vomiting (PONV) after orthognathic surgery: a retrospective study and literature review. J Oral Maxillofac Surg. 2006 Sep;64(9):1385-97. doi: 10.1016/j.joms.2006.05.024.
Results Reference
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PubMed Identifier
19453311
Citation
Grover VK, Mathew PJ, Hegde H. Efficacy of orally disintegrating ondansetron in preventing postoperative nausea and vomiting after laparoscopic cholecystectomy: a randomised, double-blind placebo controlled study. Anaesthesia. 2009 Jun;64(6):595-600. doi: 10.1111/j.1365-2044.2008.05860.x.
Results Reference
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PubMed Identifier
20532102
Citation
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Citation
Oksuz H, Zencirci B, Ezberci M. Comparison of the effectiveness of metoclopramide, ondansetron, and granisetron on the prevention of nausea and vomiting after laparoscopic cholecystectomy. J Laparoendosc Adv Surg Tech A. 2007 Dec;17(6):803-8. doi: 10.1089/lap.2006.0243.
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Citation
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Janicki PK, Sugino S. Genetic factors associated with pharmacotherapy and background sensitivity to postoperative and chemotherapy-induced nausea and vomiting. Exp Brain Res. 2014 Aug;232(8):2613-25. doi: 10.1007/s00221-014-3968-z. Epub 2014 May 4.
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Results Reference
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Prophylactic Antiemetic Efficacy of Palonosetron Versus Ondansetron for the Prophylaxis of Postoperative Nausea and Vomiting (PONV) in Women Over 60 Years Undergoing Laparoscopic Cholecystectomy

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