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Clinical Trials/NCT01811199
NCT01811199UnknownNot Applicable

Dexamethasone Reduces Postoperative Emesis by Decreasing PGF2α and LTC4 Levels

Marmara University1 site in 1 country100 target enrollmentStarted: February 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
100
Locations
1
Primary Endpoint
Number of participants will be evaluated to show effect of dexamethasone in reducing postoperative emesis

Study Overview

Brief Summary

Hypothesis: Dexamethasone reduces postoperative emesis in thyroidectomy and mastectomy patients.

Detailed Description

This study has been done to further study the effectiveness of dexamethasone in the prevention of postoperative emesis after breast and thyroid surgery and at the same time, the mechanism of action was investigated. In this prospective, randomized controlled trial it was hypothesized that corticosteroids exert their antiemetic effects in postoperative period via plasma prostaglandin F2 alpha (PGF2 α) and plasma leukotriene C4 (LTC4) inhibition.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • breast and thyroid cancer patients no neoadjuvant treated no NSAID or steroid usage heallthy volunteers, signed the informed consent

Exclusion Criteria

  • ones who did not sign the consent form NSAID or steroid users

Outcomes

Primary Outcomes

Number of participants will be evaluated to show effect of dexamethasone in reducing postoperative emesis

Time Frame: up to 3 days

participants will be followed for the duration of hospital stay, till they are discharged in avarage 3 days for postoperative emesis.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

A.Ozdemir Aktan

professor of surgery

Marmara University

Study Sites (1)

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