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A study of two nasal sprays dexmedetomidine and butorphanol to reduce heart and blood pressure rise during anaesthesia for surgery

Intranasal Dexmedetomidine versus Intranasal Butorphanol in attenuation of haemodynamic response during laryngoscopy and intubation. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/095706
Enrollment
80
Registered
2025-10-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: K806- Calculus of gallbladder and bile duct with cholecystitis Health Condition 2: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere

Interventions

Intervention1: Intranasal Dexmedetomidine versus Intranasal Butorphanol in attenuation of haemodynamic response during laryngoscopy and intubation.: Haemodynamic response during laryngoscopy & intubat

Sponsors

Post Graduate Institute of Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA I/II 2. Either sex 3. 18 to 60 years of age 4. Elective general surgeries under general anaesthesia

Exclusion criteria

Exclusion criteria: 1. Patients not willing to participate in study 2. Any allergy to study drugs 3. Patients having comorbidities like cardiac disease & another organ dysfunction

Design outcomes

Primary

MeasureTime frame
Comparison of hemodynamic response (HR, BP) between the two groups during laryngoscopy and intubation. Timepoint: During laryngoscopy and intubation.

Secondary

MeasureTime frame
Secondary Objectives: 1. To compare the adverse effects of both the drugs when administred via intranasal route. 2. To compare the dose reduction of IV induction agent i.e. propofol during induction of general anaesthesia. 3. To compare the MAC reduction of inhalational anaesthetics by observing haemodynamics of patient during surgery. 4. To compare sedation via Ramsay sedation score before induction & after extubation. 5. To compare VAS score after extubation. 6. Time to first rescue analgesia. Timepoint: During Perioperative period

Countries

India

Contacts

Public ContactSAHIL GARG

PGIMER, Satellite Centre, Sangrur (Pb)

sahilgarg79@gmail.com9877619896

Outcome results

None listed

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