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Comparison of a thermometable tracheal tube and nasopharyngeal thermometry in patients undergoing urological surgery: a prospective observational study

Comparison of a thermometable tracheal tube and nasopharyngeal thermometry in patients undergoing urological surgery: a prospective observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099254
Enrollment
Unknown
Registered
2025-03-20
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

None

Interventions

Control subjects:Temperature measurement using nasopharyngeal temperature probe
Experimental group:Measurement of temperature using a thermo-capable airway tube

Sponsors

Hangzhou First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) patients undergoing elective urological surgery in our hospital from April 2025 to April 2026 were selected as clinical trial subjects; (2) 30 min <= expected duration of surgery <= 4 h; (3) no gender restriction; (4) age 18-85 years old; (5) 18 kg/m^2 <= body mass index (BMI) <= 29 kg/m^2; (6) ASA classification ?-? Grade

Exclusion criteria

Exclusion criteria: (1) Presence of severe respiratory disease; (2) People with severe damage to target organs such as liver, kidney, heart and brain; (3) History of difficult airway disease; (4) Have used or are using medications that interfere with thermoregulation within 1 month; (5) Temperature is not in the normal range before induction of anaesthesia, i.e., higher than 37.5°C or lower than 36.0°C; (6) Nasopharyngeal lesions or a history of surgery (7) Thyroid function abnormalities (8) History of upper respiratory tract infection with cough or sputum within 2 weeks (9) Temperature probe falling off >= 2 times in a row or data loss >15% of the time window

Design outcomes

Primary

MeasureTime frame
Consistency analysis of results with multiple measurements by Bland-Altman comparison;Surgical time;

Secondary

MeasureTime frame
Differences in temperature over time;Subgroup analyses of low, ambient, and high temperature ranges, age, and sex;Incidence of intraoperative hypothermia;Intraoperative haemorrhage;Volume of intraoperative irrigation fluid;Postoperative patient awakening time;Incidence of postoperative chills;Patient comfort (presence of sore throat, hoarseness, nosebleeds, etc.);Length of hospitalisation;

Countries

China

Contacts

Public ContactYaqin Huang

Hangzhou First People's Hospital

1021648643@qq.com+86 158 5824 3148

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026