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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04403191
Other study ID # ICU-10-20
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 10, 2019
Est. completion date February 10, 2020

Study information

Verified date March 2020
Source King Abdul Aziz Specialist Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To compare and evaluate the antiemetic effect and the safety of ondansetron, inhalational isopropyl alcohol and super hydration on adult patients after laparoscopic appendectomy.


Description:

This prospective double-blind study done on 240 patients admitted to surgical I.C.U after laparoscopic appendectomy. Those who had preoperative Koivuranta vomiting score of more than 3 enrolled in our study. Every group contains 80 patients. Patients of group A received ondansetron 4 mg intravenous immediately once reached to I.C.U and another same dose after 6 hours while patients of group B received isopropyl alcohol 70% inhalation every 15 min for 4 times then repeated after 6 hours. The last group C received intravenous normal saline at rate of 20 ml/kg over 30 minute and repeated by the same dose after 6 hours. The duration of the study was 24 hours post-operatively. As PONV is self-limited within 24 hours.


Recruitment information / eligibility

Status Completed
Enrollment 240
Est. completion date February 10, 2020
Est. primary completion date February 4, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

postoperative nausea and vomiting

Exclusion Criteria:

systemic disease as diabetes or hypertension local gastric diseases

Study Design


Related Conditions & MeSH terms

  • to Treat the Vomiting Frequently Occur Post-laparoscopic by Different Anti Emetic Drugs
  • Vomiting

Intervention

Drug:
Ondansetron
ondansetron 4 mg intravenous immediately once reached to I.C.U and another same dose after 6 hours while patients of group
isopropyl alcohol 70% inhalation
inhalation every 15 min for 4 times then repeated after 6 hours
Procedure:
laparoscopic appendectomy
all patients received post operatively after laparoscopic appenectomy

Locations

Country Name City State
Saudi Arabia King abd el Aziz specialist hospital Taif

Sponsors (1)

Lead Sponsor Collaborator
King Abdul Aziz Specialist Hospital

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary numbers of vomiting attacks numbers of vomiting attacks recorded every 15 minutes for one day for one day