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A clinical trial to study the comparative efficacy of two different doses of intravenous labetalol in patients with controlled high blood pressure

Efficacy of Two Different Doses of Labetalol Hydrochloride for Attenuation of Haemodynamic Response to Laryngoscopy and Endotracheal Intubation in Controlled Hypertensive Patients â?? Prospective Randomized Double Blind Comparative Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/12/016791
Enrollment
60
Registered
2018-12-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: I10- Essential (primary) hypertension

Interventions

Intervention1: NA: NA Intervention2: Injection Labetalol Hydrochloride: In this study, we are comparing the efficacy of two different doses of Labetalol Hydrochloride in attenuation of haemodynamic r

Sponsors

SSG Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: We include ASA grade II patients posted for planned surgery under general anasthesia requiring orotracheal intubation and having controlled hypertension.

Exclusion criteria

Exclusion criteria: Patients who refuse to give consent. Pregnant and lactating women. Anticipated difficult airway and obesity(BMI >35). Patient having allergy to study drug. Patient with sick sinus syndrome (including sino-atrial block),second or third degree heart block and persistent bradycardia ( Patients is having history of taking medication for any sort of illness like verapamil, diltiazem, digitalis glycosides, clonidine, monoamineoxidase inhibitors (except MOA-B inhibitors) and beta blocker. Patient with systemic diseases like cardiovascular, respiratory diseases like bronchial asthma and COPD, neurological, psychological, hepatic, untreated phaeochromocytoma,renal disease (diagnosed by clinical judgments and investigations) and on medication of above mentioned diseases. Time more than 20s or requiring more than two attempts for laryngoscopy and intubation.

Design outcomes

Primary

MeasureTime frame
Both doses of Labetalol Hydrochloride are expected to attenuate hemodynamic response to laryngoscopy and intubation in dose dependent manner in controlled hypertensive patients.Timepoint: Both doses of Labetalol Hydrochloride attenuate hemodynamic response to laryngoscopy and intubation in dose dependent manner in early 20 minutes after doing airway instrumentation in controlled hypertensive patients.as this first this few minutes is very crucial causing complication like myocardial ischemia and cerebrovascular events we will observe the response for this early minutes after airway instrumentation.

Secondary

MeasureTime frame
To study the different side effect of study drugTimepoint: we will obeserve various complication like bradycardia,hypotension,any cardiac arrythmia in the patient till after the giving study drug to the complition of operative procedure.

Countries

India

Contacts

Public ContactDr Komal Modi

Baroda Medical College

komaltmodi@gmail.com9712998276

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026