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COMPARISON OF BEST PROBABLE DOSE OF PROPOFOL FOR LARYNGEAL MASK AIRWAY (LMA)INSERTION CONDITIONS USING ADJUVANT DRUGS(FENTANYL OR DEXMEDETOMIDINE)IN GIVING GENERAL ANAESTHESIA IN ADULT PATIENTS

COMPARATIVE EVALUATION OF EFFECTIVE DOSE 50 OF PROPOFOL IN ADULT PATIENTS WITH SALINE-PROPOFOL, DEXMEDETOMIDINE-PROPOFOL AND FENTANYL-PROPOFOL FOR LARYNGEAL MASK AIRWAY INSERTION

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/08/004921
Enrollment
100
Registered
2014-08-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- ASA I & II

Interventions

Intervention1: DEXMEDETOMIDINE(1mcg/kg), FENTANYL(1and2mcg/kg), PROPOFOL (IN INCREMENTAL/DECREMENTAL DOSE): DEXMEDETOMIDINE(1mcg/kg) or FENTANYL(1AND2mcg/kg)EITHER OF THEM(as per group) WILL BE GIVEN

Sponsors

SAFDARJUNG HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA GRADE I&II WEIGHT 35-80KGS OR BMI OF PATIENTS WHO GIVE INFORMED WRITTEN CONSENT PATIENTS FOR ELECTIVE SURGICAL PROCEDURES

Exclusion criteria

Exclusion criteria: PATIENTS WITH HISTORY OF GERD DIFFICULT AIRWAY MALLAMPATTI SCORE >2 PATIENTS WITH CERVICAL SPINE DISEASE MOUTH OPENING OBESE PATIENTS WITH BMI >30KG/M2 PATIENTS WITH CARDIOVASCULAR DISEASE

Design outcomes

Primary

MeasureTime frame
MEAN ARTERIAL PRESSURE, HEART RATE, OXYGEN SATURATION, END TIDAL CARBON DIOXIDETimepoint: BASELINE T0, END OF ADJUVANT DRUG INJECTION T1, AFTER PROPOFOL INJECTION T2, 1 AND 3 MIN POST LMA INSERTION T3,T4

Secondary

MeasureTime frame
BRADYCARDIA HR LESS THAN 30%OF BASELINE FOR MORE THAN 1 MIN. APNOEA, MOVEMENT TO INSERTIONTimepoint: DURING ADJUVANT DRUG INFUSION, AT THE TIME OF LMA INSERTION

Countries

India

Contacts

Public ContactDR RAMA WASON

SAFDARJUNG HOSPITAL

nupur4@hotmail.com9818049948

Outcome results

None listed

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