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Preadministration of 6 percent Hydroxy ethyl starch before induction with propofol for reduction of pain on propofol injection.

A prospective interventional study to find out the effect of pre administration of 6 percent Hydroxyethyl starch for reduction of pain on propofol injection in patients undergoing general anaesthesia in Department of Anaesthesia SMS Medical College jaipur - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067424
Enrollment
130
Registered
2024-05-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: 3- Administration

Interventions

Intervention1: 6% Hydroxy ethyl Starch before 1% propofol with 2% lignocaine: Pre-administration of 100 ml of 6% hydroxy ethyl starch and observe its effect on reduction of pain on propofol 2mg/kg iv

Sponsors

Department of anaesthesiology SMS medical college jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing elective surgery under general anaesthesia. Patients willing to give written informed consent. ASA grade 1 and 2.

Exclusion criteria

Exclusion criteria: Patients with history of allergy to propofol or hydroxy ethyl starch Patients with pre-existing renal or hepatic dysfunction. Patients with cardiovascular disease,hypertension,diabetes. Emergency surgeries

Design outcomes

Primary

MeasureTime frame
To compare the incidence of pain on propofol injection between the study groupsTimepoint: 0 second 10 second. 20 second. before loss of verbal contact

Secondary

MeasureTime frame
To compare the severity of pain on propofol injection between the study groupsTimepoint: 0 second. 10 second. 20 second. before loss of verbal contact

Countries

India

Contacts

Public ContactMamta Sharma

SMS Medical College and Hospital, Jaipur

kanchan2371@yahoo.com8107872222

Outcome results

None listed

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