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UnknownNCT02386059

Prevention of Postoperative Nausea and Vomiting in Patients Undergoing Vitrectomy Under Local Anesthesia

A Multicenter Randomized Trial to Evaluate the Efficacy and Safety of Three Different Prophylactic Treatments of Postoperative Nausea and Vomiting in Patients Undergoing Vitrectomy Under Local Anesthesia

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
1,200 (estimated)
Sponsor
University of Catania · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Vitreoretinal surgery is associated with a considerable incidence of postoperative nausea and vomiting (PONV), which is reported to be as high as 60%. Reasons for this high incidence may be the long duration of surgery and anesthesia and the high degree of manipulation of the eye. Postoperative vomiting after vitrectomy is an important risk factor for the onset of several complications, such as suprachoroidal hemorrhage, with disastrous visual consequences. To date there is no evidence as to the possible protective effect of anti-emetic therapy with regard to interventions of vitrectomy performed under local anesthesia. In this prospective, randomized, multicenter, double blind study, we evaluated the efficacy of Ondansetron alone, Dexamethasone alone and in combination in controlling nausea and vomiting in patients undergoing vitrectomy under local anesthesia.

Detailed description

Patients were randomly stratified to receive 1 of 4 prophylactic antiemetic treatments (3 pharmaceutical treatment and 1 placebo) in a double-blind manner at the start of the surgery and 15 minutes before the end of surgery. The syringes were prepared by a third, neutral person not involved in the perioperative care of the patient, immediately before the start of anesthesia. All vitrectomy surgeries were performed, in each unit,under local anesthesia by a retrobulbar block. Each patients was observed and treated during a period of 24 hours after the surgery. For patients who have nausea and vomiting despite the antiemetic prophylaxis, will be given a rescue dose of 4 mg ondansetron IV.

Conditions

Interventions

TypeNameDescription
DRUGPLACEBOreceived normal saline, intravenously
DRUGDexamethasone4 mg, intravenously, at the start of surgery
DRUGOndansetron4 mg, intravenously, 15 minutes before the end of surgery.
DRUGDexamethasone + Ondansetron4 mg dexamethasone, intravenously at the start of surgery and 4 mg ondansetron intravenously 15 minutes before the end of surgery.

Timeline

Start date
2015-03-01
Primary completion
2015-08-01
Completion
2015-09-01
First posted
2015-03-11
Last updated
2015-03-11

Locations

4 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT02386059. Inclusion in this directory is not an endorsement.