The effectiveness of prophylactic antiemetics 'syouhangekabukuryouto' on postoperative nausea and vomiting patients

UMIN ID: UMIN000018381

Registered date:01/08/2015

Basic Information

• Recruitment status: Complete: follow-up complete
• Health condition(s) or Problem(s) studied: women who will receive laparoscopic gynecologic surgery
• Date of first enrollment: 2015/08/15
• Target sample size: 20
• Countries of recruitment: Japan
• Study type: Interventional

Intervention(s)

Syouhangekabukuryouto 3g
lactose 3g

Outcome(s)

• Primary Outcome: To determine whether Shohangekabukuryouto prevent PONV over 24 hours after laparoscopic gynecologic surgery

Key inclusion & exclusion criteria

• Age minimum: 20years-old
• Age maximum: 60years-old
• Gender: Female
• Exclude criteria: Patients who will receive an emergency operation Patients who have allergic reaction to drugs Patients who used prophylactic antiemetic drugs whithin 24 hours before operation Patients who used analgetic drugs whithin 24 hours before operation Patients who have used Chinese harb Patients who is lactose intolerant Patients who we couldn't get a consent form

Related Information

• Primary Sponsor: Saiseikai Central Hospital
• Source(s) of Monetary Support: Saiseikai Central Hospital Anesthesiology