NCT07450768

Brief Summary

This study looked at whether a person's emotional personality type affects how they experience pain and how well a regional anesthesia technique works during arm surgery. We studied patients who underwent wrist or upper arm surgery using an axillary nerve block (a type of regional anesthesia that numbs the arm). Before surgery, patients completed a questionnaire measuring their emotional temperament, including anxious, depressive, cyclothymic, irritable, and other personality traits. We found that patients with an anxious personality type were more likely to need conversion to general anesthesia during surgery. They also reported higher pain scores after surgery. Patients with depressive traits also experienced higher pain levels. In contrast, some other temperament types reported lower pain levels. These findings suggest that emotional characteristics may influence how patients respond to anesthesia and pain after surgery. Understanding a patient's temperament before surgery may help doctors better plan anesthesia, provide additional support when needed, and improve overall comfort and safety. This research supports a more personalized approach to anesthesia care, taking into account not only physical health but also psychological factors.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
46

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 15, 2023

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 15, 2024

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

March 1, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 5, 2026

Completed
Last Updated

March 5, 2026

Status Verified

March 1, 2026

Enrollment Period

1 year

First QC Date

March 1, 2026

Last Update Submit

March 1, 2026

Conditions

Keywords

affective temperamentTEMPS-AAxillary brachial plexus blockConversion to general anesthesiaPostoperative pain

Outcome Measures

Primary Outcomes (1)

  • Anesthesia Escalation (Sedation and/or General Anesthesia)

    Proportion of patients who required escalation beyond axillary brachial plexus block, defined as the need for additional intravenous sedation and/or conversion to general anesthesia due to inadequate surgical anesthesia or patient discomfort.

    Intraoperative period (from block performance until completion of surgery)

Secondary Outcomes (2)

  • Postoperative Pain Intensity (VAS Score)

    Preoperative baseline, postoperative 3rd hour, 12th hour, and 24th hour

  • Predictors of Anesthesia Escalation

    Intraoperative period

Study Arms (6)

Depressive Temperament Group

Patients classified as having a depressive affective temperament based on TEMPS-A questionnaire scoring. Procedure: Axillary Brachial Plexus Block Ultrasound-guided axillary brachial plexus block performed using 20 mL of 0.25% bupivacaine for surgical anesthesia of the upper extremity. Drug: Intravenous Sedation Supplemental intravenous sedation administered intraoperatively in cases of patient discomfort during regional anesthesia. Sedation was provided according to standard institutional practice. Procedure: General Anesthesia (if required) Conversion to general anesthesia when regional anesthesia with or without sedation was insufficient to maintain adequate surgical conditions. Block failure was defined as inability to complete the procedure under regional anesthesia alone.

Anxious Temperament Group

Patients classified as having an anxious affective temperament according to TEMPS-A assessment. Procedure: Axillary Brachial Plexus Block Ultrasound-guided axillary brachial plexus block performed using 20 mL of 0.25% bupivacaine for surgical anesthesia of the upper extremity. Drug: Intravenous Sedation Supplemental intravenous sedation administered intraoperatively in cases of patient discomfort during regional anesthesia. Sedation was provided according to standard institutional practice. Procedure: General Anesthesia (if required) Conversion to general anesthesia when regional anesthesia with or without sedation was insufficient to maintain adequate surgical conditions. Block failure was defined as inability to complete the procedure under regional anesthesia alone.

Cyclothymic Temperament Group

Patients identified with cyclothymic temperament characteristics using TEMPS-A. Procedure: Axillary Brachial Plexus Block Ultrasound-guided axillary brachial plexus block performed using 20 mL of 0.25% bupivacaine for surgical anesthesia of the upper extremity. Drug: Intravenous Sedation Supplemental intravenous sedation administered intraoperatively in cases of patient discomfort during regional anesthesia. Sedation was provided according to standard institutional practice. Procedure: General Anesthesia (if required) Conversion to general anesthesia when regional anesthesia with or without sedation was insufficient to maintain adequate surgical conditions. Block failure was defined as inability to complete the procedure under regional anesthesia alone.

Hyperthymic Temperament Group

Patients classified as hyperthymic temperament type based on questionnaire results. Procedure: Axillary Brachial Plexus Block Ultrasound-guided axillary brachial plexus block performed using 20 mL of 0.25% bupivacaine for surgical anesthesia of the upper extremity. Drug: Intravenous Sedation Supplemental intravenous sedation administered intraoperatively in cases of patient discomfort during regional anesthesia. Sedation was provided according to standard institutional practice. Procedure: General Anesthesia (if required) Conversion to general anesthesia when regional anesthesia with or without sedation was insufficient to maintain adequate surgical conditions. Block failure was defined as inability to complete the procedure under regional anesthesia alone.

Irritable Temperament Group

Patients identified as having irritable temperament features according to TEMPS-A scoring. Procedure: Axillary Brachial Plexus Block Ultrasound-guided axillary brachial plexus block performed using 20 mL of 0.25% bupivacaine for surgical anesthesia of the upper extremity. Drug: Intravenous Sedation Supplemental intravenous sedation administered intraoperatively in cases of patient discomfort during regional anesthesia. Sedation was provided according to standard institutional practice. Procedure: General Anesthesia (if required) Conversion to general anesthesia when regional anesthesia with or without sedation was insufficient to maintain adequate surgical conditions. Block failure was defined as inability to complete the procedure under regional anesthesia alone.

Non-Dominant Temperament Group

Patients who did not demonstrate dominance in any of the five primary temperament categories. Procedure: Axillary Brachial Plexus Block Ultrasound-guided axillary brachial plexus block performed using 20 mL of 0.25% bupivacaine for surgical anesthesia of the upper extremity. Drug: Intravenous Sedation Supplemental intravenous sedation administered intraoperatively in cases of patient discomfort during regional anesthesia. Sedation was provided according to standard institutional practice. Procedure: General Anesthesia (if required) Conversion to general anesthesia when regional anesthesia with or without sedation was insufficient to maintain adequate surgical conditions. Block failure was defined as inability to complete the procedure under regional anesthesia alone.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of adult patients undergoing elective upper extremity surgery at Kırşehir Ahi Evran University Training and Research Hospital, a tertiary academic medical center in Turkey. Participants were recruited from patients evaluated in the preoperative anesthesia outpatient clinic and scheduled to receive ultrasound-guided axillary brachial plexus block as the primary anesthetic technique.

You may qualify if:

  • Age between 18 and 65 years
  • Scheduled for elective upper extremity surgery requiring axillary brachial plexus block
  • American Society of Anesthesiologists (ASA) physical status I-III
  • Ability to understand and complete the TEMPS-A questionnaire
  • Provision of written informed consent

You may not qualify if:

  • Refusal to participate
  • Contraindication to regional anesthesia (e.g., local infection at injection site, coagulopathy)
  • Known allergy to local anesthetics (bupivacaine)
  • Cognitive impairment or inability to complete the temperament questionnaire
  • Severe psychiatric disorder requiring active treatment
  • Incomplete perioperative data or missing VAS assessments

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ahi Evran University

Kırşehir, 40100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Wounds and InjuriesPain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asssistant Professor

Study Record Dates

First Submitted

March 1, 2026

First Posted

March 5, 2026

Study Start

March 15, 2023

Primary Completion

March 15, 2024

Study Completion

March 15, 2024

Last Updated

March 5, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be made publicly available. De-identified data may be made available from the corresponding author upon reasonable request, subject to institutional and ethical approval.

Locations