ClinicalTrials.gg
Not yet recruitingNCT06273319Updated Feb 22, 2024

The Effect of Oxygen Application With Double Nasal Cannula on Respiratory Complications

An interventional study of OXYGEN THERAPY in Gastric Disease and Gastric Distress, sponsored by Inonu University. Not yet recruiting at 1 site in Turkey. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2024-02-22.

Sponsored by Inonu University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by May 2024, 2 years 6 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

To compare desaturation and respiratory complications by applying oxygen therapy with double nasal cannula to patients who are planned to undergo gastrointestinal endoscopy.

Read the detailed description

Two groups of patients scheduled for gastrointestinal endoscopy will be compared in terms of desaturation and respiratory complications by applying 15 litres of oxygen therapy to the first group and 30 litres to the second group with double nasal cannula.

02

Conditions studied

  • Gastric Disease
  • Gastric Distress

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Keywords

  • Desaturation
  • oxygen therapy
  • Sedoanalgesia
03

In context

Stomach Diseases

53 studies on the registry are indexed under Stomach Diseases; 6 are open to participants now.

This study's planned enrollment of 200 is above the median of 75 across 39 interventional studies indexed under Stomach Diseases.

Browse Stomach Diseases studies →

Lead sponsor

Inonu University is the lead sponsor of 394 studies on the registry; 95 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

18-65 years old

PATIENTS WHO WILL HAVE ENDOSCOPY AND OR COLONOSCOPY

Exclusion criteria

Exclusion Criteria:

  • Having low saturation Lung cancer
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
200 participants (estimated)

Study arms

  • Placebo comparator
    Group 1: Patients who will receive 15 litres oxygen therapy

    : Patients who will receive 15 litres oxygen therapy, will be applied throughout the transaction.Patient saturation and complications such as bronchospasm and laryngospasm respiratory arrest will be recorded throughout the procedure.

    Drug: OXYGEN THERAPY

  • Active comparator
    Group 2: Patients who will receive 30 litres oxygen therapy

    Patients who will receive 30 litres oxygen therapy,will be applied throughout the transaction.Patient saturation and complications such as bronchospasm and laryngospasm respiratory arrest will be recorded throughout the procedure.

    Drug: OXYGEN THERAPY

Interventions

  • DrugOXYGEN THERAPY

    15 AND 30 LT OXYGEN TREATMENT

06

What researchers measure

Primary outcomes

  1. Determination of the amount of oxygen to prevent the peripheral oxygen saturation of the patients from falling below 95%

    Determination of the amount of oxygen to prevent the peripheral oxygen saturation of the patients from falling below 95%

    Time frame: Up to 24 weeks

07

Study locations

1 site
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Mar 2024; primary completion for May 2024, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 12, 2024
First posted
Feb 22, 2024
StartEst.
Mar 15, 2024
Primary completionEst.
May 1, 2024
CompletionEst.
Jun 1, 2024
Last update
Feb 22, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 22, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06273319
Lead sponsor
Inonu University
Responsible party
DUYGU DEMİROZ (Principal Investigator, Inonu University) — Principal investigator
First posted
Feb 22, 2024
Start date
Mar 15, 2024 (estimated)
Primary completion
May 1, 2024 (estimated)
Completion
Jun 1, 2024 (estimated)
Last update
Feb 22, 2024

Study contacts

DUYGU DEMIROZ, dr
Contact
drduygudemiroz@hotmail.com
+905319504421

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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