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Recovery of patients after sleep dose of Propofol vs Dexmedetomidine

Recovery Characteristics in patients undergoing short gynecological day care procedure under sedation with Dexmedetomidine vs Propofol : Double Blind randomized Controlled Trial. - Sedation,Daycare,Dexmedetomidine,Propofol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/09/009795
Enrollment
17
Registered
2017-09-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

None listed

Interventions

Intervention1: propofol: Sedative ,Hypnotic agent Intervention2: Dexmedetomidine: selective alpha-2-adrenergic receptor agonist.sedative, analgesic, and respiratory sparing properties Intervention3: p

Sponsors

Mahatma Gandhi medical college and research institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients ASA1 and 2 scheduled for elective short day care gynaecological surgery duration < 30Min under Iv sedation

Exclusion criteria

Exclusion criteria: Patients with known allergies to any of the test drugs,pregnancy,Drug abuse,chronic pain condition,Difficult airway, BMI > 35,Neurological disorder,psychological disorder

Design outcomes

Primary

MeasureTime frame
Modified Aldrete score,Finger Taper Test,Visual spatial memory Test,Timepoint: Modified Aldrete score every 1 min till score 9-10,Finger Taper Test and Visual spatial memory Test every hour till 4 hour—

Secondary

MeasureTime frame
Heart rate, mean arterial blood pressure,Respiratory Rate and SpO2,Sedation score Timepoint: Heart rate, mean arterial blood pressure,RR and SpO2 (Baseline,Every two minute for 10 minutes,Then every 5 minutes until the end of surgery) Sedation scores assessment (Every two minute for 10 minutes,Then every 5 minutes until the end of surgery)—

Countries

India

Contacts

Public Contactindubalamaurya

SBV university

indubalam@mgmcri.ac.in7639769237

Outcome results

None listed

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