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Nociception Level Index After Brachial Plexus Block In Upper Extremity Surgery: Prospective Comparison Trial

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

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. However, objective physiologic markers reflecting sympathetic modulation remain limited. Forty five adults undergoing upper extremity surgery with BPB and general anesthesia, bilateral NoL monitoring will be performed during local anesthetic injection, endotracheal intubation, and nasogastric tube placement. The primary aim to investigate whether the brachial plexus block induces unilateral modulation of post-operative nervous system activity, assessed by inter-limb differences in NoL values during predefined nociceptive stimuli under general anesthesia. The secondary aim to evaluate the correlation between postoperative metrics, postoperative pain intensity, and analgesic consumption. From a clinical perspective, bilateral autonomic monitoring may offer a novel adjunctive method for intraoperative confirmation of block activity, particularly in sedated or anesthetized patients where traditional sensory testing is not feasible. Furthermore, inter-limb autonomic gradients could represent a future research pathway for objective assessment of regional anesthesia effectiveness beyond subjective pain scores.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Age \>18

• Upper extremity surgery

• Provision of signed and dated informed consent forms

Locations
Other Locations
Israel
Carmel medical center
RECRUITING
Haifa
Contact Information
Primary
Michael Grach, DR.
Grachm@gmail.com
+972506265753
Backup
Dana Kosh, Dr.
danak@clalit.org.il
972-48250785
Time Frame
Start Date: 2023-03-28
Estimated Completion Date: 2026-09-30
Participants
Target number of participants: 45
Treatments
patient both arms: one operated under brachial plexus block, other serves only as control;
Related Therapeutic Areas
Sponsors
Leads: Carmel Medical Center

This content was sourced from clinicaltrials.gov