Comparison of Ultrasound-guided Brachial Plexus Blocks and Selective Distal Blocks in Terms of Anesthesia

Sponsor
Samsun University (Other)
Overall Status
Completed
CT.gov ID
NCT05656625
Collaborator
(none)
2
1
9
6.8

Study Details

Study Description

Brief Summary

Ultrasound-guided brachial plexus blocks (infraclavicular, axillary) can be applied as the main anesthetic method in hand and wrist surgeries, as well as single or combination block applications of the median, radial and ulnar nerves at the forearm level.

Here, we aimed to retrospectively evaluate the perioperative and postoperative data of patients who underwent hand and wrist surgery under distal nerve blocks and brachial plexus blocks in our hospital.

Condition or Disease Intervention/Treatment Phase
  • Other: descriptive

Detailed Description

The retrospective files of patients who used ultrasound guided regional anesthesia techniques as the main anesthetic method in hand and wrist surgeries in our hospital between 01.01.2021 and 01.09.2022 will be examined. Patients over the age of 18 who go to hand and wrist surgery will be included. Patients who have undergone surgical intervention in more than one region in the same session and who have psychiatric disorders that will affect the perception of pain will be excluded from the study. Demographic characteristics, American Society of Anesthesiology (ASA) scores, comorbidity, block performed (distal peripheral nerve block and/or brachial nerve block) and volume applied, block performance time, first analgesia times, surgery times, surgery types, discharge times, additional The existence of the complaint will be recorded. The data obtained by grouping the patients according to the type of anesthesia applied (brachial plexus block and distal nerve blocks) will be subjected to statistical analysis.

Study Design

Study Type:
Observational
Actual Enrollment :
2 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Comparison of Ultrasound-guided Brachial Plexus Blocks and Selective Distal Blocks in Terms of Anesthesia Success and Discharge Time in Hand and Wrist Surgeries: A Single Center, Historic Cohort Study
Actual Study Start Date :
Dec 20, 2022
Actual Primary Completion Date :
Dec 29, 2022
Actual Study Completion Date :
Dec 29, 2022

Arms and Interventions

Arm Intervention/Treatment
group distal nerve block(DNB)

Radial, median and ulnar nerve blocks were used alone or in combinations as a method of anesthesia for patients who had undergone hand and wrist surgery.

Other: descriptive
The block performed (distal peripheral nerve block and/or brachial nerve block) and the volume applied, block performance time, first analgesia times, surgery times, surgery types, discharge times, presence of additional complaints will be recorded. The data obtained by grouping the patients according to the type of anesthesia applied (brachial plexus block and distal nerve blocks) will be subjected to statistical analysis.

group brachial plexus block(BPB)

Brachial plexus blocks (infraclavicular, axillary etc.) was applied to patients who were going to undergo hand and wrist surgery.

Other: descriptive
The block performed (distal peripheral nerve block and/or brachial nerve block) and the volume applied, block performance time, first analgesia times, surgery times, surgery types, discharge times, presence of additional complaints will be recorded. The data obtained by grouping the patients according to the type of anesthesia applied (brachial plexus block and distal nerve blocks) will be subjected to statistical analysis.

Outcome Measures

Primary Outcome Measures

  1. Quality in Anaesthesia [up 24 hours]

    The patients were called by phone and asked to evaluate the anesthesia technique used in their surgery. Three main judgments including 'quality of anesthesia', 'whether they would prefer the same anesthesia again' and 'whether they would recommend this technique to others' were evaluated with a 5-point Likert scale. 5 point Likert scale consists of 5 answer options which will contain two extreme poles and a neutral option connected with intermediate answer options. In evaluation of parient satisfaction, we used 5 point Likert scale example to measure satisfaction is: (1) Very dissatisfied, (2)Dissatisfied, (3) Neither satisfied nor dissatisfied, (4) Satisfied , (5)Very satisfied . In other terms, (1) Strongly disagree; (2) Disagree; (3) Neither agree nor disagree; (4) Agree; (5) Strongly agree.

Secondary Outcome Measures

  1. discharge time [up to 24 hours]

    The time of discharge will be specified in both groups.

  2. block performance time [intraoperative]

    Block performance time was defined as the time from ultrasound probe insertion to needle removal at the end of perineural injections.

  3. additional anesthetic/analgesic requirement [perioperative period]

    additional analgesic requirement will be evaluated intraoperatively or postoperatively.

  4. complications [up to 24 hours]

    The presence of complications will be evaluated during and after the block.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients over the age of 18 who go to hand and wrist surgery will be included.
Exclusion Criteria:
  • Patients who have undergone surgical intervention in more than one region in the same session and who have psychiatric disorders that will affect the perception of pain will be excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsun University Samsun Ilkadım Turkey 55100

Sponsors and Collaborators

  • Samsun University

Investigators

  • Principal Investigator: gamze MD ertaş, specialist, Samsun University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gamze Ertas, principle investigator, Samsun University
ClinicalTrials.gov Identifier:
NCT05656625
Other Study ID Numbers:
  • distal block
First Posted:
Dec 19, 2022
Last Update Posted:
Dec 30, 2022
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Gamze Ertas, principle investigator, Samsun University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 30, 2022