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NCT02947672 Clinical Trial

Intravenous Versus Intra-peritoneal Dexamethasone on the Incidence of Postoperative Nausea and Vomiting

Postoperative Nausea and Vomiting Clinical Trial

Official title:
Effect of Intravenous Versus Intra-peritoneal Dexamethasone on the Incidence of Postoperative Nausea and Vomiting Following Laparoscopic Gynecological Surgeries

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02947672
Other study ID # 01003060377
Secondary ID
Status Completed
Phase N/A
First received October 24, 2016
Last updated February 11, 2018
Start date November 2016
Est. completion date November 2017

Study information
Verified date February 2018
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Effect of intravenous versus intra-peritoneal dexamethasone on the incidence of postoperative nausea and vomiting following Laparoscopic gynecological surgeries.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date November 2017
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

1. Adult Female patients

2. American society of anesthesiologist class I & II

3. Undergoing Laparoscopic gynecological surgeries

Exclusion Criteria:

1. Patient refusal to participate in the study

2. Patients with coagulopathy or under anticoagulation therapy.

3. Infection near the site of needle insertion.

4. Body mass index > 40kg/m2

5. Patients with any neurological or neuromuscular disorder or history of seizures.

6. Known allergy to any drug used in the study.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Intravenous Dexamethasone

• Intraperitoneal Dexamesathone

Locations
Country Name City State
Egypt Assiut University Hospital Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative nausea and vomiting (PONV) PONV will be measured by using Verbal Descriptive Scale 24 hours
Secondary Pain Pain will be assessed by using visual analogue scale 24 hours
See also
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