Postoperative Nausea and Vomiting Clinical Trial
Official title:
The Effects of Intravenous Fosaprepitant and Ondansetron for the Prevention of Postoperative Nausea and Vomiting in Thoracicsurgery Patients: A Single-center, Randomized, Double-Blinded Clinical Study
The goal of this clinical trial is to compare the efficacy, safety and feasibility of intravenous Fosaprepitant and Ondansetron for the prevention of postoperative nausea and vomiting in thoracicsurgery patients. Participants will be randomized in a 1:1 ratio to the Fosaprepitant and Ondansetron group.The groups were analyzed and compared for frequency of vomiting in 24 h after surgery. In addition, we will further compare the occurrence of postoperative pulmonary complications, length of hospital stay, nutrition and quality of life after surgery in patients treated with different antiemetic prophylaxis.
Status | Not yet recruiting |
Enrollment | 234 |
Est. completion date | June 2023 |
Est. primary completion date | June 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: 1. aged between 18 and 70 years 2. physical status classified by the American Society of Anesthesiologists (ASA) scale as I to III 3. Apfel score = 2 4. undergoing thoracoscopic pneumonectomy Exclusion Criteria: 1. Preoperative disorders of consciousness 2. body mass index (BMI) > 35 kg/m2 3. occurrence of episodes of nausea or vomiting within 24 h prior to surgery?motion sickness,?previous PONV?people who smoke?people with alcoholism?use of corticosteroids, psychoactive or antiemetic drugs,?hypersensitivity to the study medications 4. serious kidney, liver, lung, heart, brain or bone marrow disease 5. conversion from thoracoscopic pneumonectomy to conventional pneumonectomy 6. participation in another clinical study. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Qilu Hospital of Shandong University |
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Gan TJ, Belani KG, Bergese S, Chung F, Diemunsch P, Habib AS, Jin Z, Kovac AL, Meyer TA, Urman RD, Apfel CC, Ayad S, Beagley L, Candiotti K, Englesakis M, Hedrick TL, Kranke P, Lee S, Lipman D, Minkowitz HS, Morton J, Philip BK. Fourth Consensus Guidelines for the Management of Postoperative Nausea and Vomiting. Anesth Analg. 2020 Aug;131(2):411-448. doi: 10.1213/ANE.0000000000004833. Erratum In: Anesth Analg. 2020 Nov;131(5):e241. — View Citation
Gan TJ, Diemunsch P, Habib AS, Kovac A, Kranke P, Meyer TA, Watcha M, Chung F, Angus S, Apfel CC, Bergese SD, Candiotti KA, Chan MT, Davis PJ, Hooper VD, Lagoo-Deenadayalan S, Myles P, Nezat G, Philip BK, Tramer MR; Society for Ambulatory Anesthesia. Consensus guidelines for the management of postoperative nausea and vomiting. Anesth Analg. 2014 Jan;118(1):85-113. doi: 10.1213/ANE.0000000000000002. Erratum In: Anesth Analg. 2014 Mar;118(3):689. Anesth Analg. 2015 Feb;120(2):494. — View Citation
Gan TJ, El-Molem H, Ray J, Glass PS. Patient-controlled antiemesis: a randomized, double-blind comparison of two doses of propofol versus placebo. Anesthesiology. 1999 Jun;90(6):1564-70. doi: 10.1097/00000542-199906000-00011. — View Citation
Hata A, Okamoto I, Inui N, Okada M, Morise M, Akiyoshi K, Takeda M, Watanabe Y, Sugawara S, Shinagawa N, Kubota K, Saeki T, Tamura T. Randomized, Double-Blind, Phase III Study of Fosnetupitant Versus Fosaprepitant for Prevention of Highly Emetogenic Chemotherapy-Induced Nausea and Vomiting: CONSOLE. J Clin Oncol. 2022 Jan 10;40(2):180-188. doi: 10.1200/JCO.21.01315. Epub 2021 Nov 18. — View Citation
Hesketh PJ, Van Belle S, Aapro M, Tattersall FD, Naylor RJ, Hargreaves R, Carides AD, Evans JK, Horgan KJ. Differential involvement of neurotransmitters through the time course of cisplatin-induced emesis as revealed by therapy with specific receptor antagonists. Eur J Cancer. 2003 May;39(8):1074-80. doi: 10.1016/s0959-8049(02)00674-3. — View Citation
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of PONV within 24 hours | The groups will be analyzed and compared for frequency of nausea and vomiting in 24 h after surgery | Day 1 | |
Secondary | Incidence of PONV within 48 hours | The groups will be analyzed and compared for frequency of nausea and vomiting in 48 h after surgery | Day 2 | |
Secondary | occurrence of Drug-related adverse effects | The groups will be compared for the incidence of unwanted effects of antiemetic medicines include onstipation,weakness, headache, dizziness and sleepiness. | Day 3 | |
Secondary | Postoperative pain score | This project will be measured by patients' postoperative pain score. | Day 3 | |
Secondary | The dosage of opioids used after surgery | This project will be measured by the dosage of opioid drugs used after surgery. | Day 3 | |
Secondary | the length of hospital stay | The groups will be compared for the time from admission to discharge | From date of admission until the date of discharge, assessed up to 7 days. | |
Secondary | postoperative pulmonary complications | Postoperative pulmonary complications include respiratory infection,respiratory failure,pleural effusion,atelectasis and pneumothorax | Day 3 |
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