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Comparison of effect of ketamine and lidocaine on prevention of emergence agitation in Rhinoplasty

Phase 3
Recruiting
Conditions
rhinoplasty surgery.
Intraoperative and postprocedural complications and disorders of the respiratory system, not elsewhere classified
J95-J95
Registration Number
IRCT20220302054164N1
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
72
Inclusion Criteria

Referral for elective rhinoplasty surgery
Age 18-45 years
Lack of known allergies to the drugs used in the present study
No pregnancy
No drug addiction
Do not use psychotropic drugs
Perform surgery under general anesthesia
Classification of ASA class, I-II

Exclusion Criteria

Taking painkillers and sedatives 24 hours before surgery
History of heart disease, nervous system, and neurological disorders
Patient with a history of previous rhinoplasty
History of seizures
Duration of anesthesia and surgery more than 2 hours

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Restlessness when waking up from anesthesia. Timepoint: During anesthesia until the end of the patient's presence in the recovery room, the patient's vital signs will be measured. Also, during the presence at recovery, the RASS and NRS questionnaires will be filled in. Method of measurement: After extubation and transfer of the patient to recovery room, the patient's restlessness will be recorded by the RASS scale every 10 minutes until discharge from the recovery by a trained nurse who does not know the patient group. Also, after transferring the patient to recovery room, the amount of postoperative pain will be recorded by the Numerical Pain Measurement Scale (NRS) every 10 minutes.
Secondary Outcome Measures
NameTimeMethod
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