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Compare the effect of heated humidified high flow nasal cannula to prevent hypothermia then unhumidified oxygen through venturi mask in patients undergoing transurethral procedure under neuraxial anesthesia

Effect of heated humidified high flow nasal Oxygen on core body temperature compared to the venture mask in patients undergoing transurethral procedure under neuraxialanaesthesia:- a randomized clinical trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/047455
Enrollment
100
Registered
2022-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: D303- Benign neoplasm of bladder Health Condition 2: D291- Benign neoplasm of prostate Health Condition 3: T68- Hypothermia Health Condition 4: C679- Malignant neoplasm of bladder, unspecified Health Condition 5: C689- Malignant neoplasm of urinary organ, unspecified Health Condition 6: 4- Measurement and Monitoring Health Condition 7: O- Medical and Surgical Health Condition 8: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system

Interventions

Intervention1: Heated Humidified High Flow Nasal Cannula: Compare the Effect of heated humidified high flow nasal oxygen with Venturi mask on core body temperature in ttransurethral procedures under n

Sponsors

Department of anesthesia and intensive care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Posted for transurethral resection of bladder tumour/ transurethral resection of prostate Neuraxial anesthesia

Exclusion criteria

Exclusion criteria: Requiring General anesthesia/Failed neuraxial anesthesia Haemodynamic unstable patients Febrile on arrival to OT Signs of sepsis or thrombophlebitis

Design outcomes

Primary

MeasureTime frame
Difference in proportion of patients with tympanic temperature 36 degree c at least once during the procedure.Timepoint: From beginning of anesthesia till end of the surgery

Secondary

MeasureTime frame
Change in Axillary temperature between baseline and end of procedureTimepoint: From beginning of anesthesia till end of the surgery;Change in Tympanic temperature between baseline and end of procedure. Timepoint: From beginning of anesthesia till end of the surgery.;Incidence of ShiveringTimepoint: Perioperative;Patient satisfaction (at 0 hours post surgery on a 7 point GPE)Timepoint: 0 hours to postoperative;Total oxygen flow required(calculated from the mean intraoperative gas flow and mean set FiO2)Timepoint: From beginning of anesthesia till end of the surgery

Countries

India

Contacts

Public ContactVishally Dhingra

PGIMER Chandigarh

bjfiero@gmail.com8427561868

Outcome results

None listed

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