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COMPARING 6 PERCENT HYDROXYETHYL STARCH AND 2 PERCENT LIGNOCAINE IN REDUCING PAIN FROM PROPOFOL INJECTION

COMPARISION OF 6 PERCENT HYDROXYETHYL STARCH TO 2 PERCENT LIGNOCAINE PRETREATMENT ON PREVENTION OF PAIN ON PROPOFOL INJECTION -A RANDOMISED CONTROLLED STUDY - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089862
Enrollment
94
Registered
2025-06-30
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: HYDROXYETHYL STARTCH: 6 percent Hydroxyethyl startch 100 ml infused over 5 minutes will be given following which patient will be premedicated and induced with injection propofol and pai

Sponsors

Deparrment of anaesthesiology JLN medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I and II weight 40kg to 80kg patient undergoing elective surgery under General anaesthesia

Exclusion criteria

Exclusion criteria: known hypersensitive reaction to study drug contraindication to Lignocaine, hydroxyethyl startch, propofol emergency surgeries presence of left ventricular dysfunction

Design outcomes

Primary

MeasureTime frame
Incidence of pain on propofol injectionTimepoint: every 5 to 10 seconds till loss of verbal contact—

Secondary

MeasureTime frame
to compare severity of pain on propofol injection between the study groups haemodynamic changes adverse events if anyTimepoint: every 5 to 10 seconds till loss of verbal contact—

Countries

India

Contacts

Public ContactDr ARVIND KHARE

Jawahar Lal Nehru medical college

arvindkhare68@gmail.com9414306114

Outcome results

None listed

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