Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06040034
Other study ID # AN-202309.01
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date February 2, 2023
Est. completion date May 1, 2023

Study information

Verified date September 2023
Source Universitas Padjadjaran
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this randomized controlled trial is to compare the effect of lidocaine bolus intravenous administration to lidocaine continuous intravenous administration in post thyroidectomy patients to observe the effect against post-extubation cough. The main questions it aims to answer are: - Cough incidence on both groups - Which method is preferable to reduce post-extubation cough incidence


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date May 1, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - ASA class 1 and 2 - Thyroidectomy patients in Hasan Sadikin Bandung Hospital Exclusion Criteria: - Subjects' refusal - Had history of drug allergy, specifically lidaocaine - Had history of asthma or other lung diseases - Active smoker - History of arrhythmia - Bradycardia subjects (<60 beats per minute) - Pregnant people - Perioperative upper respiratory tract infusion - Routinely consume ACE inhibitor / bronchodilators / steroid - Renal dysfunction - Liver dysfunction

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Lidocaine IV
Lidocaine given as bolus or continuous infusion.

Locations

Country Name City State
Indonesia Hasan Sadikin General Hospital Bandung West Java

Sponsors (1)

Lead Sponsor Collaborator
Universitas Padjadjaran

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Post-Extubation Cough Grade Cough graded according to the following criteria:
Grade 0: no cough; Grade 1: mild, only 1 cough; Grade 2: moderate, >1 cough lasting <5 seconds; Grade 3: coughing heavily and continuously for >5 seconds)
24 hours post operative
Secondary Number of participant experiencing tachycardia Tachycardia is defined as heart rate >100 beats per minute 24 hours perioperative
Secondary Number of participant experiencing bradycardia Bradycardia is defined as heart rate <60 beats per minute 24 hours perioperative
Secondary Number of participant experiencing hypertension Increase of blood pressure >20% from initial blood pressure 24 hours perioperative
Secondary Number of participant experiencing hypotension Decrease of blood pressure <20% from initial blood pressure 24 hours perioperative
See also
  Status Clinical Trial Phase
Completed NCT00116337 - Spinal Cord Stimulation to Restore Cough N/A
Not yet recruiting NCT04064333 - Slow-Stream Expiratory Muscle Strength Training for Veterans With Dysphagia Living in Long-term Care N/A
Recruiting NCT02482818 - Efficacy of Pregabalin on Chronic Cough Phase 1/Phase 2
Terminated NCT02269761 - Chest Ultrasound of ER Patients With Cough or SOB
Active, not recruiting NCT02065440 - The Effect of Ebastine/Pseudoephedrine on Subacute Cough N/A
Completed NCT01071161 - The Effect of Azithromycin in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Chronic Productive Cough Phase 3
Terminated NCT00668317 - Bronchial Hyper-responsiveness in Reflux Cough Phase 3
Completed NCT00353951 - An Observational Study of Cough / Lower Respiratory Tract Infection (LRTI) in Primary Care N/A
Completed NCT00127686 - Effect of Honey and Dextromethorphan on Nocturnal Cough and Sleep Phase 1
Completed NCT00287339 - The Utility of Nexium in Chronic Cough and Reflux Disease Phase 4
Recruiting NCT05115097 - AI Evaluation of COVID-19 Sounds (AI-EChOS)
Recruiting NCT04457011 - Efficacy and Safety of Susu Zhike Granules for Treating Acute Cough Due to Common Cold With Cold-cough Syndrome in Children Phase 2
Recruiting NCT05042063 - Acoustic Cough Monitoring for the Management of Patients With Known Respiratory Disease
Recruiting NCT03922373 - A Study of Benzonatate Soft Capsule in Chinese Healthy Subjects Phase 1
Completed NCT05812209 - Stellate Ganglion Block to Treat Long COVID 19 Case Series
Recruiting NCT04767074 - A Non-pharmacological Cough Control Therapy N/A
Recruiting NCT05570539 - Assessment of the Pharmacokinetics of BLU-5937 Extended Release Prototypes and a BLU-5937 Immediate Release Reference Formulation Phase 1
Completed NCT03999203 - A Cross-sectional Study to Measure Cough in Severe Asthma N/A
Active, not recruiting NCT05479929 - Work of Breathing Assessment in Triage Scale
Recruiting NCT02495571 - Assessment of Voluntary and Reflex Cough in Patients With ALS N/A