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Compares treatment options for Analgesics, Opioid
Official title Asleep Fiberoptic vs Direct Laryngoscopy Effect on Hemodynamic Stability Using Opioid Free Anesthesia Induction
ClinicalTrials.gov ID: NCT06487988
What this study is testing
- What it's testing
- The goal of this clinical trial is to compare blood pressure and heart rate between the fiberoptic and direct oral intubation using opioid free anesthesia induction. Secondary objectives include comparing the time needed for intubation and the incidence of postoperative sore throat, hoarseness, and upper airway trauma in adults aging between 18 to 55 years, scheduled for elective surgery under general anesthesia.
- Time commitment: about 1 year
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 55. Healthy volunteers may be eligible.
You may be able to join if
- ASA (American Society of Anesthesiologists) physical status I and II
- Range age of 18-55 years' old
- Scheduled for elective surgery under general anesthesia.
You likely can't join if
- History of cardiovascular diseases.
- History of lung disease.
- Hypertensive patient (BP\> 140/90)
- Patient taking medications that affect blood pressure and heart rate
- Morbid obesity (BMI \>30)
- Severe GERD
See the full eligibility criteria
- ASA (American Society of Anesthesiologists) physical status I and II
- Range age of 18-55 years' old
- Scheduled for elective surgery under general anesthesia.
- History of cardiovascular diseases.
- History of lung disease.
- Hypertensive patient (BP\> 140/90)
- Patient taking medications that affect blood pressure and heart rate
- Morbid obesity (BMI \>30)
- Severe GERD
- Predicted difficult airway (Short TMD \ III)
- Neck instability
- Patient planned to receive rapid sequence intubation
- Patient refusal to participate
- History of difficult intubation/ ventilation
The study team makes the final eligibility decision.
Where it's taking place
- Beirut, Lebanon
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 1 year per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 55 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Beirut, Lebanon. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.