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Studying the efficacy of using lidocaine and dexmedetomidine as an alternative to propofol to provide sedation for patients undergoing colonoscopy.

Testing the efficacy of Lidocaine and dexmedetomidine as an alternative to propofol for sedation in colonoscopy according to the patient satisfaction.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12620000249954
Enrollment
62
Registered
2020-02-26
Start date
2020-03-01
Completion date
2020-11-28
Last updated
2021-07-05

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

Conditions

None listed

Brief summary

Colonoscopy is one of the most common day case procedures allover the world. Propofol has been the gold standard drug used for sedation and anesthesia for such cases. In our trial we will examine the efficacy of using dexmedetomidine and lidocaine infusion as an alternative to propofol infusion in such cases

Interventions

Patients scheduled for colonoscopy will be devided into two groups to receive either sedation by propofol infusion or by combined dexmedetomidine and lidocaine. (A) propofol infusion at dose 25-75 ug/kg/min, Lidocaine infusion 1-2 mg/kg/hour and Dexmedetomidine infusion 0.2-0.5 ug/kg/min, all the infusions will start just before the beginning of the procedure. (B) Drugs will be administered all-through the duration of the procedure (C) Drugs will be administered by intravenous infusion (D) Th

Patients scheduled for colonoscopy will be devided into two groups to receive either sedation by propofol infusion or by combined dexmedetomidine and lidocaine. (A) propofol infusion at dose 25-75 ug/kg/min, Lidocaine infusion 1-2 mg/kg/hour and Dexmedetomidine infusion 0.2-0.5 ug/kg/min, all the infusions will start just before the beginning of the procedure. (B) Drugs will be administered all-through the duration of the procedure (C) Drugs will be administered by intravenous infusion (D) The primary anesthesiologist ( the anesthesiologist who planned the methodology ) will be responsible for administration. (E) The group who will receive lidocaine and Dexmedetomidine will be the intervention group

Sponsors

NMC Royal Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
19 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

All adult ASA I and II patients admitted for elective colonoscopy

Exclusion criteria

Patients with bradycardia (heart rate < 55/min). Patients with known allergy to. lidocaine or dexemedotimidine

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026