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Nasotracheal Tube Stenting by Nelaton Catheter in Pediatric Dental Surgery

A

Ain Shams University

Status

Completed

Conditions

Anesthesia Intubation Complication

Treatments

Device: Nelaton catheter
Device: Endotracheal tube

Study type

Interventional

Funder types

Other

Identifiers

NCT03462732
FAMSU R 6 / 2018

Details and patient eligibility

About

The value of this study is to compare between stented endotracheal tube with nelaton catheter and non stented tube as regard nasotracheal related complications as epistaxis and nasal cavity injury.

Enrollment

80 patients

Sex

All

Ages

3 to 9 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pediatric patients scheduled for dental surgery under general anesthesia age 3-9 years
  • physical status American society of Anesthesiologist(ASA) I orII

Exclusion criteria

  • History of recurrent epistaxis
  • Coagulopathy
  • Previous nasal surgery
  • History of nasal trauma
  • Severe renal , hepatic or cardiovascular disease
  • History of drug allergy to the drugs used in the study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups

Group I
Active Comparator group
Description:
Endotracheal tube plus Nelaton catheter
Treatment:
Device: Endotracheal tube
Device: Nelaton catheter
Group II
Active Comparator group
Description:
Endotracheal tube
Treatment:
Device: Endotracheal tube

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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