FindTrial
Sign In

We are comparing how rocuronium and vecuronium will reduce the complications of succinylcholine by giving them before it.

COMPARATIVE STUDY OF PRETREATMENT OF ROCURONIUM VS VECURONIUM ON POST SUCCINYLCHOLINE COMPLICATIONS IN ELECTIVE SURGERIES.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021820
Enrollment
140
Registered
2019-10-30
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: O- Medical and Surgical

Interventions

Intervention1: ROCURONIUM: AFTER PRE MEDICATING THE PATIENT,0.05mg/kg OF ROCURONIUM WILL BE GIVEN 90SECONDS PRIOR TO SUCCINYLCHOLINE. Control Intervention1: VECURONIUM: AFTER PRE MEDICATING THE PATIEN

Sponsors

B KRISHNA PREETHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA: Adult patients of either sex between 18-60yrs. Patients of American society of anaesthesiologists(ASA) grade I and II physical status. Patient posted for elective surgeries under general anaesthesia of duration atleast 30min.

Exclusion criteria

Exclusion criteria: 1.BMI > 30 2.History of allergy to any particular drug used in the study 3.History of egg allergy 4.History of substance abuse 5.Pregnancy 6.Post burn, post trauma, and other hyperkalemic states

Design outcomes

Primary

MeasureTime frame
To reduce the undesirable side effects of succinylcholine like fasciculations and post operative myalgia.Timepoint: INTRAOPERATIVELY 90 SECONDS AFTER GIVING SUCCINYLCHOLINE AND POST OPERATIVELY DAY 1 2 AND 3—

Secondary

MeasureTime frame
TO PROVIDE BETTER INTUBATING CONDITIONS INTRA OPERATIVELY.Timepoint: 60-90seconds after completion of succinylcholine action.—

Countries

India

Contacts

Public ContactDR DEBASIS DEBATA

Kalinga Institute of Medical Sciences

debasisdebata@gmail.com9937344446

Outcome results

None listed

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