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A study to assess the effect of thermal softening of endotracheal tube in reducing post operative sore throat

A Prospective, Randomized case control study to evaluate the effect of thermal softening of endotracheal tube in reducing post operative sore throat

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/040813
Enrollment
270
Registered
2022-03-04
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Thermal softening of endotracheal tube: Endotracheal tube will be placed in sterile saline which is at 40.C for 10 minutes Control Intervention1: Control group: Endotracheal tube will b

Sponsors

RajaRajeswari Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who give written informed consent. Patients aged 18-60 yrs. Patients scheduled for elective surgery under General anesthesia ( Patients with ASA (American society of anesthesiologists) grade I & II

Exclusion criteria

Exclusion criteria: Patients refusing to participate in the study. Patients having ongoing acute infections. Patients with preoperative sore throat Patients with electrolyte abnormalities. Patients with hepatic and renal dysfunction. Patients with chronic alcohol abuse. Patients on long term analgesic therapy. Patients with history of endocrine disease inclusive of diabetes mellitus. Morbid obesity, chronic use of steroids or immunosuppressant or recent chemotherapy. Patients with difficult airway. Pregnant and lactating patents.

Design outcomes

Primary

MeasureTime frame
To evaluate the effect of thermal softening of endotracheal tube in reducing post operative sore throat. Timepoint: Sore throat will be evaluated for one hour, six hours and twenty four hours in the post operative period

Secondary

MeasureTime frame
To evaluate for cough and hoarseness of voice in post operative period. side effects(if any) Timepoint: One hour, six hours, twenty four hours after surgery

Countries

India

Contacts

Public ContactChaithali H

RajaRajeswari Medical College and Hospital

chaithali.acharya@gmail.com9972674755

Outcome results

None listed

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