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Postoperative Nausea and Vomiting: Ramosetron Plus Aprepitant vs Palonosetron Plus Aprepitant

K

Kyungpook National University

Status

Completed

Conditions

Postoperative Nausea and Vomiting

Treatments

Drug: Ramosetron
Drug: palonosetron
Drug: aprepitant

Study type

Interventional

Funder types

Other

Identifiers

NCT02597907
KNUH 2014-05-016

Details and patient eligibility

About

The purpose of this study was to compare the antiemetic efficacy of aprepitant plus palonosetron versus aprepitant plus ramosetron in high risk patients undergoing laparoscopic cholecystectomy.

Full description

The purpose of this study was to compare the antiemetic efficacy of aprepitant plus palonosetron versus aprepitant plus ramosetron in high risk patients undergoing laparoscopic cholecystectomy.

Study is performed during 24 hours after surgery.

Enrollment

88 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Non smoking, female patients, scheduled for laparoscopic cholecystectomy

Exclusion criteria

  • Patients with gastrointestinal disorder,
  • Patients with allergies to any study medication,
  • Patients who had received any sedatives, opioid, steroid or antiemetics within 24 h before surgery

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

88 participants in 2 patient groups

aprepitant plus palonosetron
Experimental group
Description:
aprepitant 80 mg palonosetron 0.075 mg
Treatment:
Drug: aprepitant
Drug: palonosetron
aprepitant plus ramosetron
Active Comparator group
Description:
aprepitant 80 mg ramosetron 0.3 mg
Treatment:
Drug: Ramosetron
Drug: aprepitant

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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