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Effect of remifentanyl on intubation response in hyper tensive patients.

Comparison of the effect of remifentanil versus dexmedetomidine on stress response to laryngoscopy in hypertensive patients undergoing surgery under general anaesthesia: a prospective, randomised, double-blind study. - nil

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072528
Enrollment
100
Registered
2024-08-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: inj remifentanyl: patients in Group R will receive IV remifentanil as 1 mcg/kg bolus over 45 sec followed by 0.2 mcg/kg/min. Control Intervention1: inj dexmeditomidine: Patients in Grou

Sponsors

Dr Annu Choudhary
Lead Sponsor
Dr Swati Singh
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Primary Hypertension Grade 1 & 2, ASA II, posted for elective surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: • Patient’s refusal to participate • Uncompensated cardiovascular, pulmonary, neurological, hepato-renal, endocrine disorders • Allergy to study drugs • Any substance abuse disorders. • Viral marker status positive

Design outcomes

Primary

MeasureTime frame
change in BIS values on laryngoscopyTimepoint: immediately after intubation (Ti)

Secondary

MeasureTime frame
Comparison of time to achieve BIS 50 in between two groups 2. Comparison of total propofol consumption for induction in between the two groups 3. Incidence of any adverse effects in two groups 4. Comparison of change in vital parameter ( HR, MAP,SpO2, RR) Timepoint: Baseline (0min) 1 min 2 min 3 min 4 min 5 min 6 min 7 min 8 min 9 min 10 min Before induction After induction Before laryngoscopy After intubation (Ti) 5 min 10 mins 30 min 60 min end of surgery

Countries

India

Contacts

Public ContactDr Annu Choudhary

Indira Gandhi institute of medical sciences, Patna

anucdry@gmail.com7385161632

Outcome results

None listed

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