Which drug wins? labetalol vs lignocaine for safer intubation in gallbladder surgery
NCT ID NCT07192081
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether labetalol or lignocaine (lidocaine) is better at preventing sudden rises in heart rate and blood pressure when a breathing tube is inserted for gallbladder surgery. 116 adults having elective laparoscopic gallbladder removal will receive one of the two drugs before intubation. The goal is to see which keeps vital signs more stable, helping anesthesiologists choose the safer option.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- labetalol and lignocaine (lidocaine)
- What this could lead to
- If one drug works better, it could become the preferred choice for keeping patients stable during intubation for gallbladder surgery.
- What could go wrong
- This is a small, early-stage trial (116 people) comparing two common drugs. Results may not apply to other surgeries or patients with health problems.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 116 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Feb 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * ASA Grade I and II * Age 18 to 60 years * Elective laparoscopic cholecystectomy * Both genders * Informed consent given Exclusion Criteria: * Hypersensitivity to labetalol/lignocaine * Hypertensive on antihypertensives * ASA Grade III or more * Cardiovascular, renal, hepatic, or endocrine issues * Pregnant/lactating * BMI ≥ 35 * Anticipated difficult airway
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hayatabad Med Complex
RECRUITINGPeshawar, Khyber Pakhtunkhwa, 25000, Pakistan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Could a sleep drug shield older hearts from post-surgery delirium?
- How do countries train anesthesia residents? a global snapshot