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NCT01945502 Clinical Trial

Nasopharyngeal Packing and Rhinologic Surgery.

PONV Clinical Trial

Official title:
The Effectiveness of Three Different Nasopharyngeal Packing on the Prevention of Postoperative Nausea- Vomiting and Postoperative Throat Pain in Rhinologic Surgery.

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01945502
Other study ID # 11-434-13
Secondary ID
Status Recruiting
Phase N/A
First received September 16, 2013
Last updated September 16, 2013
Start date September 2013

Study information
Verified date September 2013
Source Ankara University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess the efficacy of three different pharyngeal packing during routine rhinologic surgery in the prevention of postoperative nausea and vomiting, and to evaluate the influence of pharyngeal packing on postoperative throat pain.

Recruitment information / eligibility
Status Recruiting
Enrollment 120
Est. completion date
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- 18-60 years old adult patient

- nasal and/or paranasal sinus surgeries

- general anesthesia

Exclusion Criteria:

- patients submitted to another intervention at the same time (adenoidectomy, tonsillectomy)

- patients with a serious systemic disease (acquired immunodeficiency syndrome,leukemia, lymphoma, or other neoplasias under chemotherapy treatment)

- patients presenting contraindications for using nonsteroid anti-inflammatory drugs

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Ankara University Faculty of Medicine ENT operating rooms Ankara

Sponsors (1)
Lead Sponsor Collaborator
Basak Ceyda MECO

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative nausea vomiting 3 months No
Primary sore throat 3 months No
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