Anesthesia Clinical Trial
Official title:
A Novel Co-induction Technique Compared to Standard Inhalational and Intravenous Induction Techniques: a Prospective Randomized Control Study
Verified date | February 2020 |
Source | University of Jordan |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Co-induction technique refers to the use of a combination of medications to reach the desired therapeutic target. In the present study, the investigators examined the safety of a novel co-induction approach that relied on a simple timing and dosing alterations to the classical approaches of inhalational sevoflurane and propofol induction. The significance of this study is to find a reliable safe alternative method of induction that can provide optimal parameters,when compared to the classical methods of induction.
Status | Completed |
Enrollment | 105 |
Est. completion date | January 3, 2017 |
Est. primary completion date | January 2, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 65 Years and older |
Eligibility |
Inclusion Criteria: - patients with Age = 65 years. - American Society of Anaesthesiologists' (ASA) score II or III. - minimally invasive endoscopic urological procedures. Exclusion Criteria: - patient refusal. - Age < 65 years. - family history of malignant hyperthermia. - prolonged surgery that needed intubation. - body mass index (BMI) > 35 kg/m2. |
Country | Name | City | State |
---|---|---|---|
Jordan | Jordan University Hospital | Amman |
Lead Sponsor | Collaborator |
---|---|
University of Jordan |
Jordan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Intraoperative respiratory adverse events | The investigators recorded the occurrence of transient apnea intraoperatively, in addition to laryngeal spasm, coughing, gagging and increased salivation. The study chart included the documentation these common adverse events, the timing of occurrence, and the intervention required to manage these events. | 8 months | |
Secondary | Time for successful laryngeal mask airway insertion | The investigators assessed the time needed for LMA insertion. The timer was started upon giving the fentanyl, recording the time till successful insertion of laryngeal mask airway. | 8 months | |
Secondary | Blood pressure stability | The investigators recorded patients' blood pressure readings throughout the induction procedure. | 8 months | |
Secondary | Heart rate stability | The investigators recorded patients' heart rate throughout the induction procedure. | 8 months | |
Secondary | Changes in oxygen saturation | The investigators recorded patients' oxygen saturation throughout the induction procedure. | 8 months |
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