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study comparing between paracetamol and 6% hydroxy ethyl starch for decreasing pain induced by propofol injection during operation

A Comparative Prospective Study On Analgesic Efficacy Of Premedication With Intravenous Paracetamol Versus Intravenous 6% Hydroxy Ethyl Starch For Reduction Of Propofol Induced Pain During Induction Of General Anaesthesia In Patients Undergoing Elective Surgeries At Tertiary Care Hospital In Mandya

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052451
Enrollment
60
Registered
2023-05-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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: paracetamol: one group recieves 100ml paracetmol IV . we will be evaluating the pain score during 20 sec and for post operative complications for 24 hours Control Intervention1: 6 % hyd

Sponsors

DR KIRAN A V
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Aged between 18 to 60 years 2.ASA I and II category patients 3.Patients posted under general anaesthesia 4.Patients willing to give informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Anaphylaxis to the study drugs( 6% HES and paracetmol) 2.Chronic alcoholics and nicotine addiction 3.Patients with opioid drug intake for other comorbid conditions

Design outcomes

Primary

MeasureTime frame
To compare the effectiveness of pretreatment with i.v. paracetamol with that of 6% hydroxy ethyl starch to reduce pain induced by propofol injection.Timepoint: 0 sec , 1 sec , 2 sec , 3 sec , 4 sec , 5 sec , 10 sec , 15 sec , 20 sec—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactChidanand Halagatti

Mandya Institute of medical sciences

virupaksha2614@yahoo.com8867917802

Outcome results

None listed

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