HFNC vs Conventional Oxygen During Gastrocolonoscopy in Elderly Patients
NCT07916298, Not applicable, Not yet recruiting, Turkish Society of Anesthesiology and Reanimation
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | HFNC vs Conventional Oxygen During Gastrocolonoscopy in Elderly Patients | ClinicalTrials.gov |
| NCT number | NCT07916298 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 154 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Turkish Society of Anesthesiology and Reanimation | ClinicalTrials.gov |
| Conditions | Hypoxemia, Eldery People, Endoscopy, Colonoscopy, Apnea During Procedural Sedation | ClinicalTrials.gov |
| Interventions | HİGH FLOW NASAL CANNULA OXYGEN, NASAL CANNULA OXYGEN | ClinicalTrials.gov |
| First posted | 2026-11-04 | ClinicalTrials.gov |
| Last updated | 2026-11-04 | ClinicalTrials.gov |
Registered outcomes 4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Hypoxemia | persists for at least 10 seconds during sedation and endoscopy. | The primary outcome of the study is the occurrence of hypoxemia, defined as a peripheral oxygen saturation (SpO₂) below 90% that persists for at least 10 seconds during sedation and endoscopy. | ClinicalTrials.gov |
| Secondary | Minimum SpO₂ During the Procedure: | end of the procedure | The lowest peripheral oxygen saturation (SpO₂) value (%) recorded by pulse oximetry during sedation and endoscopy will be assessed. | ClinicalTrials.gov |
| Secondary | Total Duration of Hypoxemia | end of the procedure | The total duration (in seconds) during which SpO₂ remains below 90% during sedation and endoscopy will be recorded and compared between the two groups. | ClinicalTrials.gov |
| Secondary | Requirement for Airway Interventions | end of the procedure | Airway and respiratory support interventions performed due to hypoxemia or respiratory depression during sedation and endoscopy will be evaluated. These interventions will include the jaw-thrust maneuver, tactile or painful stimulation, repositioning of the head and neck, use of airway adjuncts, and bag-mask ventilation when necessary. The proportion of patients requiring at least one airway intervention will be compared between the two groups. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)