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The availability study of tissue oxygenation monitor in pharyngeal and tracheal mucosa

Single-center, single-arm pilot study of the feasibility of measuring oxygen saturation with a tissue oxygen saturation monitor in pharyngeal suture and permanent tracheal stoma in total laryngectomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs042220151
Enrollment
20
Registered
2023-03-01
Start date
2023-04-04
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer or severe aspiration condition requiring total laryngectomy

Interventions

Measuring the tissue oxygen saturation of the pharyngeal and tracheal mucosa using a tissue oxygen saturation monitor during laryngectomy and pharyngeal suture/permanent tracheostomy

Sponsors

Mukaigawa Takashi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for palliative or radical surgery for total laryngectomy* 2. If due to cancer, the primary site is irrelevant 3. If due to cancer, any tissue type 4. Patients who gave written informed consent before enrollment 5. Aged 18 or older at the time of obtaining consent * Including total laryngectomy to prevent aspiration due to severe aspiration

Exclusion criteria

Exclusion criteria: 1. Patients who cannot be closed with pharyngeal mucosal suture alone and will require a free flap 2.Uncontrolled diabetes mellitus 3. Unstable angina pectoris (angina pectoris with onset or exacerbation within the last 3 weeks) or history of myocardial infarction within 6 months. 4.Poorly controlled hypertension as a complication. 5.Receiving continuous systemic (oral or intravenous) steroids or other immunosuppressants 6. SPO2<90% at enrollment 7. Severe occlusive vasculopathy 8. Complications with other cancers requiring simultaneous surgery 9.In addition, patients who are considered inappropriate as subjects of this study by the judgment of the doctor

Design outcomes

Primary

MeasureTime frame
Comprehensive determination of the presence or absence of acquisition values of tissue oxygen saturation of normal mucosa away from the wound.

Secondary

MeasureTime frame
1.Results of using Tokkale 2.Presence or absence of suture failure 3.Presence or absence of tracheal necrosis 4.Presence or absence of preoperative irradiation

Contacts

Public ContactShinichi Okada

Shizuoka Cancer Center

sh.okada@scchr.jp+81-55-989-5222

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026