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Lignocaine in gastroscopy

LIG Trial - Lignocaine in gastroscopy and the effect on time to eye opening.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12620000023954
Acronym
LIG
Enrollment
100
Registered
2020-01-15
Start date
2020-06-16
Completion date
2021-11-09
Last updated
2022-01-31

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

Conditions

None listed

Brief summary

The aim of this randomised controlled trial is to determine whether the use of a therapeutic dose of lignocaine enhances elective outpatient gastroscopy episodes as measured by time to eye opening, gastroscope insertion conditions, time from patient discharge from recovery and patient comfort (measured by a pain score). Hypothesis: Lignocaine is a local anaesthetic which may assist with improved endoscope insertion conditions, less post gastroscopy discomfort and faster time to wake-up and discharge from the post-anaesthetic recovery unit (PACU).

Interventions

Intervention group: 1.5mg/kg lignocaine/lidocaine to maximum dose of 120mg as a bolus dose, prior to gastroscopy, via intravenous administration, administered by anaesthetist. The injection of the 'intervention drug' will be given prior to the induction drug of propofol, preferably as soon as IV cannula is inserted. If the gastroscopy is still proceeding after 20 minutes, a further dose of the 'intervention drug' will be given (either NaCl 0.9% or 1.5mg/kg of lignocaine not exceeding a total d

Intervention group: 1.5mg/kg lignocaine/lidocaine to maximum dose of 120mg as a bolus dose, prior to gastroscopy, via intravenous administration, administered by anaesthetist. The injection of the 'intervention drug' will be given prior to the induction drug of propofol, preferably as soon as IV cannula is inserted. If the gastroscopy is still proceeding after 20 minutes, a further dose of the 'intervention drug' will be given (either NaCl 0.9% or 1.5mg/kg of lignocaine not exceeding a total dose of 3mg/kg lignocaine). (Please note, patients who are having a simultaneous colonoscopy will not be included.) Strategies to monitor adherence: independent researcher to note that the 'intervention drug' (1x10ml syringe of 10ml NaCl 0.9% or lignocaine 1.5mg/kg up to maximum dose of 120mg bolus) is given prior to induction. A gastroscopy involves insertion of a gastroscope (a semi rigid telescope with a camera on the end) which is inserted by the gastroenterologist into the mouth and terminating in the small bowel via the stomach and oesophagus. This procedure usually done under sedation in Australia with the assistance of an anaesthetist. The procedure duration is usually under 10 minutes and rarely exceeds 30 minutes. For further information, please refer to this website:https://healthywa.wa.gov.au/Articles/F_I/Gastroscopy-endoscopy

Sponsors

Alfred health
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Adults (greater than or equal to 18 years) undergoing elective outpatient gastroscopy with low aspiration risk.

Exclusion criteria

1. Patient refusal 2 After-hours or emergency gastroscopies including indications for upper gastrointestinal bleed. 3 Contraindication or allergy to lignocaine. 4 <18 years old or >80 years old 5. Pregnant patients 6. Patients at high risk for aspiration or requiring intubation 7. Gastroscopy solely performed by topicalisation of the throat 8. Patients requiring opioids during gastroscopy

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026