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Status unknownNCT01945502Updated Sep 18, 2013

Nasopharyngeal Packing and Rhinologic Surgery.

An observational study in Nasal Surgery, Tampons and PONV, sponsored by Basak Ceyda MECO. Status unknown at 1 site in Turkey. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2013-09-18.

Sponsored by Basak Ceyda MECO · Observational

The sponsor has not verified this record recently (last verified Sep 2013), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
120
Ages
18 Years to 60 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Nasal Surgery
  • Tampons
  • PONV
03

In context

Lead sponsor

Basak Ceyda MECO is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Adult patients (18-60 years) scheduled for routine nasal and/or paranasal sinus surgeries in Ankara Univerity Faculty of Medicine, ETN operating rooms were recruited into this study.

Inclusion criteria

  • 18-60 years old adult patient
  • nasal and/or paranasal sinus surgeries
  • general anesthesia

Exclusion criteria

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
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
120 participants (estimated)
Patient registry
No

Groups and cohorts

  • nasal packing with dry packs
  • nasal packing with wet packs
  • nasal packing with Benzidamin-Clorhexsidin damped packs
  • no nasal packing
06

What researchers measure

Primary outcomes

  1. Postoperative nausea vomiting

    Time frame: 3 months

  2. sore throat

    Time frame: 3 months

07

Study locations

1 of 1 sites recruiting
  • Ankara University Faculty of Medicine ENT operating rooms
    Ankara, 06100, Turkey
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01945502
Lead sponsor
Basak Ceyda MECO
Responsible party
Basak Ceyda MECO (MD, DESA, Ankara University) — Sponsor-investigator
First posted
Sep 18, 2013
Start date
Sep 2013
Primary completion
Dec 2013 (estimated)
Last update
Sep 18, 2013

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2013. You cannot join it, but the record below documents what was studied.

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