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Opioid Free Anaesthesia for head and neck cancer surgeries

Comparison of opioid free anaesthesia versus opioid containing anaesthesia for elective head and neck cancer surgery under anaesthesia- Randomized control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049777
Enrollment
114
Registered
2023-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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

Conditions

Health Condition 1: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynx

Interventions

Intervention1: Propofol Ketamine infusion for maintenance of Anaesthesia: In opioid free group ( Group K), Patients will be given Inj. Dexmedetomidine 0.5 mcg/kg[12] bolus dose over 20 minutes prior t

Sponsors

Bhaikaka univercity
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patients american society of anesthesiologists .physical status (ASA -PS) I,II,III who can give written and informed consent, Age 18-65 years, either Gender, Patients undergoing elective head and neck cancer surgery

Exclusion criteria

Exclusion criteria: Patients who will not give consent for research ,uncontrolled systemic disease ,conduction abnormality and patient with implantable defibrillator and pacemaker ,who are allergic to study drugs ,h/o convulsion ,psychiatric disorders,renal,hepatic ,cardiac insufficiency ,who will be un-reversed and on mechanical ventilation support post operatively

Design outcomes

Primary

MeasureTime frame
To compare the post- operative analgesia in opioid free and opioid containing group of patients undergoing elective head and neck cancer surgeryTimepoint: immediate post-operative period to 1 hr,2,4,8,12,24 hours post-operative period

Secondary

MeasureTime frame
To compare haemodynamic stability in both the groups, To assess and compare post- operative sedation in these two groups of patients. ,To assess the total consumption of drugs, To assess the side effects of drugs.Timepoint: intra operative and post operative 0,1,2,4,6,12,24 hours

Countries

India

Contacts

Public ContactNirali Mavsinh Rathod

Pramukhswami Medical College

docbhum29@yahoo.com9904438877

Outcome results

None listed

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