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this is a study to minimise the post operative pain and fine muscle contractions which is seen after succinylcholine during inductions.

COMPARATIVE EVALUATION OF PROPOFOL AND THIOPENTONE TO PREVENT SUCCINYLCHOLINE INDUCED FASCICULATION AND MYALGIA IN GABAPENTINE PREMEDICATED PATIENTS: A PROSPECTIVE RANDOMISED CONTROL TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032329
Enrollment
80
Registered
2021-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: PCS- Health Condition 2: PCS-

Interventions

Intervention1: Propofol containing lipid agent.: Assessment of fasciculation and myalgia after giving intravenous dose at rate of 2mg/hr.fasciculation noted intraoperatively upto 5min and postoperativ

Sponsors

IGIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: asa grade 1 and 2, pt. undergoing for elective surgery

Exclusion criteria

Exclusion criteria: asa grade 3 or more, pt. age less than 18 or more than 60 yrs,pt.refusal to take any oral drugs,pt. with chronic opioid use, pt. wih hep b/hep c/hiv infections, history of chronic gabapentine use, pt. with contraindication to succinylcholine use.

Design outcomes

Primary

MeasureTime frame
the assessment of incidence and severity of fasciculation and myalgia in a post operative period of 24 hoursTimepoint: the assessment of incidence and severity of fasciculation and myalgia in a post operative period of 24 hours—

Secondary

MeasureTime frame
To look for total amount of tramadol use in post operative periods of 24 hrs.Timepoint: 2hrs,6hrs,12hrs,18hrs,24hrs—

Countries

India

Contacts

Public ContactDr Vinod Kumar Verma

Indira Gandhi Institute of Medical Sciences

drvvinodv@gmail.com8292000111

Outcome results

None listed

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