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Recruiting NCT06967896

Different Models of Tracheal Catheters Are Used for Female Thyroid Glands

Observational Sore Throat Tracheal Tubes With an Inner Diameter of 6.0mm Tracheal Tubes With an Inner Diameter of 6.5mm Tracheal Tubes With an Inner Diameter of 7.0mm

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Sore Throat, Tracheal Tubes With an Inner Diameter of 6.0mm, Tracheal Tubes With an Inner Diameter of 6.5mm, Tracheal Tubes With an Inner Diameter of 7.0mm. Basic parameters: 18 years — 65 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Randomized Controlled Trial Comparing Different Models of Tracheal Tube for Thyroid Surgery in Women

Overview

Objective:Compare whether the use of tracheal catheters of models 6.0 and 6.5 causes less sore throat in women after thyroid surgery compared with the traditional use of model 7.0 tracheal catheters.Methods: Investigators enrolled 180 female patients with American Society of Anesthesiologists (ASA) physical status I and III, aged 18-65 years, and scheduled for elective undergoing thyroid surgery with general anesthesia. The participants were randomly assigned into three groups(n=60 each group):Group A: Tracheal catheter group with an inner diameter of 6.0mm, Group B: Tracheal catheter group with an inner diameter of 6.5mm, Group C: Tracheal catheter group with an inner diameter of 7.0mm.The incidence and severity of postoperative sore throat were recorded in three groups at 1 h, 6 h, 24 h and 48 h after operation.

Primary outcome measures

  • The incidence of postoperative sore throat [Time frame: at 1 hour, 6 hour, 24 hour and 48 hour after operation]

Eligibility criteria

Inclusion criteria

  • Female;
  • Thyroid surgery should be performed under general anesthesia (GA) at an appropriate time;
  • ASA grade I-III;
  • Aged 18-65 years;
  • BMI less than 35Kg/m2
  • In line with ethics, patients voluntarily accept this experiment and sign informed consent.

Exclusion criteria

  • Reflux esophagitis, preoperative sore throat, chronic pharyngitis, preoperative hoarseness, use of anticoagulants or corticosteroids, high risk of reflux or aspiration, dysphagia, previous oral or pharyngeal surgical intervention, bleeding disorder, severe heart, lung, liver and kidney dysfunction
  • Upper respiratory tract infection occurred within 2 weeks before surgery
  • Unable to insert ET (no more than two intubations)
  • Patients with hoarseness or sore throat before surgery
  • Language communication, hearing impairment or brain dysfunction such as stroke, unable to communicate

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-control

Study locations

China · 1 center
  • Department of Anqing Hospital Anesthesiology — Anqing

Identifiers

NCT: NCT06967896 · Sun LingLU

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗