Nociception Level Index After Brachial Plexus Block In Upper Extremity Surgery
Recruiting
Observational Study
Brachial Plexus Blockade
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 45 (estimated)
- Sponsor
- Carmel Medical Center · Other
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About This Trial
The present prospective within-subject observational study will evaluate whether unilateral brachial plexus block (BPB) induces measurable lateralized autonomic modulation, assesses using bilateral Nociception Level (NoL) monitoring during standardized intraoperative stimuli under general anesthesia. Regional anesthesia efficacy is traditionally assessed through sensory and motor examination. Howe…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age \>18
* Upper extremity surgery
* Provision of signed and dated informed consent forms
Exclusion Criteria:
* Pregnant women
* Known allergic reaction to bupivacaine or other anesthetic medicine: Midazolam, Fentanyl, Propofol, Rocuronium, Remifentanil, Sevoflurane)
* Known…
Contacts