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Study to compare the effect of Injection Labetalol and Injection Glyceryl Trinitrate in the treatment of high blood pressure

A Randomized Controlled Open Label Prospective Study to Assess Efficacy and Safety of Intravenous Labetalol Vs Intravenous Glyceryl Trinitrate in the Management of Hypertensive Crisis - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069126
Enrollment
68
Registered
2024-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: I169- Hypertensive crisis, unspecified

Interventions

Intervention1: Intravenous Labetalol: Labetalol 20 mg given as stat dose, followed by incremental doses of 20–80 mg every 10 minute until the target BP goal is achieved. Maximum dose of labetalol will

Sponsors

KPC Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.SBP =180 mm Hg / DBP =120 mm Hg with evidence of acute end organ damage 2.Patient above 18 years of age. 3.Patient / legally acceptable representative of the patient who are willing to provide informed written consent.

Exclusion criteria

Exclusion criteria: COPD, Bradycardia , Pregnancy ,LVEF less than 35% , recent use of any intravenous beta blockers or antihypertensives or phosphodiesterase inhibitors.

Design outcomes

Primary

MeasureTime frame
Proportion of patients achieving the target MABP (reduction of the MABP by 25% from the original MABP at presentation) in the groups receiving GTN and LabetalolTimepoint: At baseline , 1 hour, 2 hours and 24 hours.

Secondary

MeasureTime frame
Systolic and Diastolic blood pressureTimepoint: 30 mins,1hour, 2 hours, 6 hours, 12 hours, 24 hours

Countries

India

Contacts

Public ContactABHIJIT KUMAR SINHA

KPC MEDICAL COLLEGE and HOSPITAL

abhijeetkumar.shina@gmail.com9681094935

Outcome results

None listed

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