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Study of Injection Sugammadex after muscle relaxation agents in Cardiac Catheterisation Laboratory

Sugammadex Versus Neostigmine: A comparative Study of Efficacy and Safety in the Cath lab

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053360
Enrollment
50
Registered
2023-06-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: Q20-Q28- Congenital malformations of the circulatory system Health Condition 2: I00-I99- Diseases of the circulatory system

Interventions

Intervention1: Sugammadex: Reversal with 2 mg/kg dose of Sugammadex after the completion of procedure and after two twitches on Train Of Four. Control Intervention1: Neostigmine: Reversal with 0.05 mg

Sponsors

Institutional Research Society
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade I-IV patients. 2. Age between 20 and 60 years. 3. Patients posted for elective cardiac catheterisation procedures in the cathlab. 4. Availability of informed consent and willingness of the patient to be a part of the study.

Exclusion criteria

Exclusion criteria: 1. Patients requiring emergency surgery. 2. Incapacity to consent 3. Patient with renal, hepatic and pre-existing pulmonary comorbidities. 4. Patients allergic to Sugammadex, neostigmine or glycopyrrolate.

Design outcomes

Primary

MeasureTime frame
Our primary outcome is to note the time(in minutes) from re-appearance of second twitch to TOF ratio more than 0.9 with sugammadex compared to neostigmine groups. This is a parameter to measure the efficacy of the study drugs.Timepoint: Baseline, Just before extubation

Secondary

MeasureTime frame
2) To measure the time to PACU discharge readiness using the modified Aldrete score in both the study groups.Timepoint: two hours after shifting to icu, four hours after shifting to icu, six hours after shifting to icu, eights hours after shifting to icu;to detect the occurrence of any adverse events after administration of study drugTimepoint: 2 hours, 4 hours, 6 hours, 8 hours

Countries

India

Contacts

Public ContactSanjeeta Umbarkar

Seth GS Medical College and KEM Hospital

sanjeeta69@yahoo.com9323273435

Outcome results

None listed

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