RANDOMIZED, DOUBLE-BLIND STUDY, CONTROLLED WITH ACTIVE COMPARATOR, OF PARALLEL GROUPS, CARRIED OUT UNDER INTERNAL BLIND CONDITIONS TO EXAMINE THE SAFETY, TOLERABILITY AND EFFECTIVENESS OF 2 DOSE OF APPRENTICATOR IN THE PREVENTION OF NAUSEA AND POST-OPERATIVE VOMITING
- Conditions
- -R11 Nausea and vomitingNausea and vomitingR11
- Registration Number
- PER-020-04
- Lead Sponsor
- MERCK SHARP & DOHME PERU S.R.L.,
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Not specified
- Target Recruitment
- 0
a. The patient is at least 18 years of age.
b. The patient is able to understand the study procedures and agrees to participate in it by providing written informed consent.
c. The patient is scheduled to undergo open abdominal surgery that requires staying in the hospital until the next day (staying 24 hours in the hospital after the end of surgery).
d. The patient is scheduled to receive general anesthesia.
a. The patient is scheduled to receive propofol for maintenance of anesthesia
b. Placement of a nasogastric or oral gastric tube intra or postoperatively.
c. The patient is allergic to pre-operative tranquillizers, operative anesthetics, postoperative analgesia, aprepitant, ondansetron or any other programmed 5-HT3 antagonist.
d. It is anticipated that the patient will receive neuraxial anesthesia, such as epidural, spinal or caudal anesthesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method