Status:
COMPLETED
Haloperidol and Dexamethasone Towards Postoperative Nausea and Pain in Adult After Laparoscopy
Lead Sponsor:
Indonesia University
Conditions:
Laparoscopy
Postoperative Nausea and Vomiting
Eligibility:
All Genders
18-65 years
Phase:
PHASE4
Brief Summary
This study aim to find out the effectiveness of 1 mg intravenous haloperidol compared to 5 mg intravenous dexamethasone to prevent the occurrence of nausea and vomiting also as pain control in adult p...
Detailed Description
Eighty subjects (n=40 for each group) scheduled for laparoscopic-assisted surgery were enrolled in a randomized double-blind clinical trial. One milligram intravenous haloperidol was given one hour be...
Eligibility Criteria
Inclusion
- underwent laparoscopic surgery (gynecology, digestive, or urology surgery)
- American Society of Anesthesiologist (ASA) physical status 1-3
Exclusion
- psychological or neurological disorders (routine haloperidol consumption)
- history of allergic reaction to dexamethasone or haloperidol
- diabetes mellitus
- did not give the consent
Key Trial Info
Start Date :
January 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 30 2020
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT05246631
Start Date
January 1 2020
End Date
July 30 2020
Last Update
February 18 2022
Active Locations (1)
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1
Cipto Mangunkusumo Central National Hospital
Jakarta Pusat, DKI Jakarta, Indonesia, 10430