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Compare oral clonidine and oral melatonin as premedication to check responses during laryngoscopy and intubation

Study to compare oral clonidine versus oral melatonin premedication on hemodynamic responce to laryngoscopy and intubation - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090884
Enrollment
152
Registered
2025-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Oral Clonidine: Oral Clonidine 0.1 mg given 90 min prior to surgery dissolved in 10 millilitres water To attenuate hemodynamic responses (heart rate and blood pressure changes) during l

Sponsors

Mahatma Gandhi Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient posted for elective surgery under General anesthesia Patient aged between 18-65 years Patient with American Society of anesthesiologists (ASA) Class I, II Consented Patients

Exclusion criteria

Exclusion criteria: Anticipated difficult intubation Pregnant and lactating females Patient receiving treatment with either of the study drug or having known case of allergy to either drugs or any drugs Patients with prolonged laryngoscopy time(more than 30 seconds) Body Mass Index (BMI) more than 30 kg/m2

Design outcomes

Primary

MeasureTime frame
to compare different effect of oral melatonin versus oral clonidine as premedication and its response changes in blood pressure , heart rate, and other relevant haemodynamic parameters during direct laryngoscopy and tracheal intubation during induction of general anesthesia in elective surgeryTimepoint: Baseline vitals followed by vitals at 5,10,15,30,60,90 minutes pre induction vitals followed by vitals at laryngoscopy followed by vitals at 5,10,15,30 minutes.

Secondary

MeasureTime frame
to evaluate any differences in side effects or adverse effects between two study groupsTimepoint: Baseline vitals and sedation score followed by vitals and sedation score at 5,10,15,30,60,90 minutes pre induction vitals followed by vitals at 5,10,15,30 minutes and postoperative vitals and sedationscoreat5,10,15,30,60 minutes.

Countries

India

Contacts

Public ContactKhayyam Moin

Mahatma Gandhi Medical College and Hospital

khayyammoin@yahoo.com9468964148

Outcome results

None listed

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