Intravenous Lidocaine Plus Intratracheal Dexmedetomidine on Postoperative Sore Throat

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAnqing Municipal Hospital

About this trial

Objective: The present study was to investigate the effect of intravenous lidocaine combined with intratracheal dexmedetomidine on postoperative sore throat in patients undergoing thyroid cancer surgery.

Methods: Investigators enrolled 144 patients with American Society of Anesthesiologists (ASA) physical status I and II, aged 18-65 years, and scheduled for elective undergoing thyroid cancer surgery with general anesthesia. The participants were randomly assigned into four groups(n=36 each group): Group L received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia. Group D received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL). Group LD received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL). Group C received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia.The incidence and severity of postoperative sore throat were recorded in four groups at 1 h, 2 h, 6 h, 24 h and 48 h after operation.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Thyroid cancer surgery with ASA grades I-II

Aged 18-65 years

The patient's communication is normal and they have a certain learning ability

Disqualifiers

Severe respiratory and circulatory system diseases

There was bradycardia (HR < 60 beats/minute) or atrioventricular block before the operation

Nervous system disease

Mental and psychological disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • Intracheal dexmedetomidine

    Drug

    Group D received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

  • Intravenous lidocaine

    Drug

    Group L received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

  • Intravenous lidocaine combined with intracheal dexmedetomidine

    Drug

    Group LD received lidocaine 1.5 mg/kg was injected intravenously 3 min before endotracheal intubation and tracheal spray with dexmedetomidine (1 μg/kg) mixed with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

  • Saline (NaCl 0,9 %) (placebo)

    Drug

    Group C received equal volume normal saline was injected intravenously 3 min before tracheal intubation and tracheal spray with 0.8% ropivacaine 40 mg (5 mL) for surface anesthesia

Treatment groups

144 Participants
are divided into 4 treatment groups
Group A: Intravenous lidocaineExperimental treatment 1 intervention
Group B: Intracheal dexmedetomidineExperimental treatment 1 intervention
Group C: Intravenous lidocaine combined with intracheal dexmedetomidineExperimental treatment 1 intervention
Group D: SalineExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The incidence and severity of postoperative sore throat

Time frame
at 1 hour, 2 hour, 6 hour, 24 hour and 48 hour after operation

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: