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Rapid Sequence Intubation With Rocuronium in Elderly Patients

Comparison of the Effect of Rocuronium Dosing Based on Ideal, Corrected or Total Body Weight on Rapid Sequence Intubation With Priming on Neuromuscular Blockage and Intubation Condition in Elderly Patients.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05067829
Enrollment
75
Registered
2021-10-05
Start date
2022-07-01
Completion date
2022-12-31
Last updated
2022-05-26

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

Conditions

Rapid Sequence Induction, Rapid Sequence Intubation, Rocuronium

Keywords

Rapid Sequence Induction and Intubation, Rapid Sequence Intubation, Rocuronium, Geriatrics

Brief summary

With the prolongation of life expectancy, the frequency of surgical intervention and anesthesia increases in elderly patients. The rapid Sequence Intubation(RSI) technique is preferred in patients with aspiration risk and who will undergo general anesthesia, especially in the pandemic period, to reduce or eliminate the aerosolization of respiratory secretions. The use of rocuronium at a dose of 1 mg/kg in RSI also causes prolongation of the recovery of neuromuscular block. This study aimed to compare the intubation conditions and train-of-four count(TOFC) 1-2 times of the rocuronium doses with priming according to ideal body weight(IBW), corrected body weight(CBW), and total body weight(TBW) in RSI of patients aged \>65 years.

Detailed description

The number of elderly patients (\>65 y) increases, and a large proportion of these patients will require surgery and anesthesia at some point. Changes in the neuromuscular junction, organ systems, and cardiac output that occur with aging cause changes in response to neuromuscular blockers. One of the reasons for rapid sequence intubation(RSI) preference is to reduce or eliminate aerosolization of respiratory secretions during general anesthesia and airway manipulation in surgical cases during the pandemic period. Guidelines regarding this subject recommend securing the airway quickly with RSI, and it is reported that aerosol production would decrease with this method. This study aimed to compare the intubation conditions and the train-of-four count (TOFC) 1 and 2 response times of the patients aged 65 and above, who were administered rocuronium at a priming dose (0.06 mg/kg) according to ideal body weight(IBW), corrected body weight(CBW), and total body weight (TBW) before induction, followed by administration of 0.94 mg/kg rocuronium 3 minutes after the anesthesia induction and intubated 45 seconds later.

Interventions

DEVICETrain of four(TOF)

Train of four(TOF) monitoring after anesthesia induction

Sponsors

Ankara City Hospital Bilkent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Intervention model description

Prospective randomized contrrolled study

Eligibility

Sex/Gender
FEMALE
Age
65 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Elective abdominal surgery * Age \> 65 years * ASA I-II -III

Exclusion criteria

* Patient with history of allergy to rocuronium * Body Mass Index \> 35 kg/m2 * Patient who had history of difficult intubation or high possibility of difficult intubation * Neuromuscular disease * Kidney failure (GFR \< 30 ml/dk/m2)

Design outcomes

Primary

MeasureTime frameDescription
The percent of excellent intubation conditionDuring intubation from start to finish of the studyScore 1: Poor jaw relaxation/ Active resistance to blade/closing vokal kord/ Severe coughing or bucking/ Vigorous limb movement Score 2: Acceptable jaw relaxation/ Intermediate vokal cord moving/ slight limb and diaphram movement score 3: relaxed laryngoscopy/ abducted vocal cords/ no limb and diphragm movement
TOF value during intubation procedureDuring intubation from start to finish of the studyTrain of four monitoring during induction and intubation
Time to TOFR equal to zeroDuring intubation from start to finish of the studyTime from rocuronium induction to TOFR equal to zero
Time to TOFC equal to 1During intubation from start to finish of the studyTime from rocuronium induction to TOFc equal to 1

Countries

Turkey (Türkiye)

Contacts

Primary ContactNadide Aysun Postacı
aysunposta@yahoo.com+905323520383

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026