Peripheral Perfusion Index as a Predictor of Successful Supraclavicular Brachial Plexus Block

NCT ID: NCT06493643

Last Updated: 2024-08-06

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 43 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-08-31
• Study Completion Date: 2024-12-31

Brief Summary

Aim of the study is to determine the best cut off value for the PI and PI ratio for predication of successful supraclavicular brachial plexus block in young and middle age patients undergoing hand surgeries .

Detailed Description

• The supraclavicular nerve block was performed under guidance of a linear transducer (8-14 MHz; Acuson x300; Siemens Healthcare, Seoul, Korea) over the supraclavicular fossa in the coronal oblique plane immediately superior to the midclavicular point. The block was induced in the semi-sitting position, with the head of the patient turned away from the side to be blocked.
• The PI was measured using Masimo SET pulse oximeter, applied on the index finger. The PI was recorded at baseline and at 10, 20, and 30min after local anaesthetic injection in both the blocked limb and the contralateral unblocked limb using two separate oximeters.
• The PI ratio was calculated as the ratio between the PI at 10min after injection and the baseline PI. In every patient, a comparison between the blocked and unblocked limb was performed.
• PI was recorded at baseline and at 10, 20, and 30 min after local anaesthetic injection in both the blocked limb and the contralateral unblocked limb.
• PI ratio was calculated as the ratio between the PI at 10 min after injection and the baseline PI.
• Vital data (Blood pressure, Heart rate, SPO2) was recorded before giving the block and at 10, 20, and 30 min after local anaesthetic injection and at the end of the operation.

Conditions

Perfusion Index

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Perfusion index at the blocked & unblocked limb

The Perfusion Index was recorded at baseline and at 10, 20, and 30 min after local anaesthetic injection in both the blocked limb and the contralateral unblocked limb using two separate oximeters.

In every patient , a comparison between the blocked and unblocked limb was performed .

Measurement of perfusion index after supraclavicular brachial plexus block at blocked & unblocked limb

Intervention Type: OTHER

The PI (Perfusion Index) was measured using Masimo SET pulse oximetry applied on the index finger. The PI was recorded at baseline and at 10 , 20 , and 30 min after local anaesthetic injection in both the blocked limb and the contralateral unblocked limb using two separate oximeters. The PI ratio was calculated as the ratio between the PI at 10min after injection and the baseline PI. In every patient, a comparison between the blocked and unblocked limb was performed .

Interventions

Measurement of perfusion index after supraclavicular brachial plexus block at blocked & unblocked limb

The PI (Perfusion Index) was measured using Masimo SET pulse oximetry applied on the index finger. The PI was recorded at baseline and at 10 , 20 , and 30 min after local anaesthetic injection in both the blocked limb and the contralateral unblocked limb using two separate oximeters. The PI ratio was calculated as the ratio between the PI at 10min after injection and the baseline PI. In every patient, a comparison between the blocked and unblocked limb was performed .

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Adult patients aging between 15_ 60 years of both sexes.
• Patients undergoing Elective hand Surgeries under successful supraclavicular brachial plexus block anesthesia.
• American Society of Anesthesiologists (ASA) physical status classes I - II.

Exclusion Criteria

• Patient's refusal of procedure or participation in the study.
• ASA classes III or above.
• Coagulopathy and bleeding disorders.
• Contraindications to supraclavicular brachial plexus block anesthesia such as local infection.
• Hypersensitivity to the study medications.
• Diabetes mellitus.
• Peripheral vascular disease.
• Emergency surgeries.

• Minimum Eligible Age: 15 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ain Shams University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

FMASU MS 726/2023

Identifier Type: -

Identifier Source: org_study_id