- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07669688
Pulse Wave Transit Time After Infraclavicular Block
Time-Dependent Changes in Pulse Wave Transit Time Following Infraclavicular Block: A Non-Invasive Assessment of Sympathetic Blockade
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Regional anesthesia success is traditionally assessed using sensory and motor block evaluation methods that rely on patient cooperation and subjective responses to external stimuli. However, these methods may be difficult to apply in sedated, uncooperative, or communication-impaired patients. Therefore, objective and non-invasive indicators of sympathetic blockade have gained increasing interest in regional anesthesia practice.
Pulse Wave Transit Time (PWTT) is defined as the time interval between the R-wave on the electrocardiogram and the arrival of the corresponding pulse wave detected by a peripheral pulse oximeter. PWTT reflects vascular tone, arterial compliance, and hemodynamic status. Sympathetic blockade induced by peripheral nerve blocks results in vasodilation and reduced vascular resistance, potentially leading to measurable changes in PWTT. Previous studies have demonstrated the utility of objective parameters such as perfusion index, skin temperature, blood flow measurements, and PWTT in assessing block success. However, data regarding the temporal changes of PWTT following infraclavicular brachial plexus block remain limited.
The primary objective of this prospective observational study is to investigate the time-dependent changes in PWTT after ultrasound-guided infraclavicular brachial plexus block. The study will be conducted in patients undergoing upper extremity surgery under infraclavicular block at Sakarya Training and Research Hospital.
Patients scheduled to receive infraclavicular block as part of their routine clinical care will be enrolled after providing informed consent. The block procedure is not performed for research purposes and represents standard clinical practice. Following block administration, PWTT values will be recorded from the blocked extremity using standard monitoring equipment. Measurements will be obtained before block placement and at 0, 5, 10, 15, and 20 minutes after block completion. Baseline PWTT measurements will also be obtained from the contralateral upper extremity.
Secondary outcome measures will include perfusion index, skin temperature of both upper extremities, heart rate, non-invasive blood pressure, respiratory rate, and oxygen saturation. Demographic and clinical data will also be recorded.
All measurements will be collected according to a predefined protocol using standardized monitoring equipment. Since PWTT is an objective device-derived parameter, observer dependency is expected to be minimal. Data collection personnel will be separated from the clinician performing the block whenever feasible to reduce measurement bias. All collected data will be anonymized prior to statistical analysis.
This study is designed as a single-center, prospective observational investigation without randomization or intervention beyond routine clinical care. The findings may contribute to the development of PWTT as a practical, objective, and non-invasive marker of sympathetic blockade following infraclavicular brachial plexus block.
Studietyp
Inskrivning (Beräknad)
Kontakter och platser
Studiekontakt
- Namn: Burçin Alaçam
- Telefonnummer: +905465903851
- E-post: burcin.ersoy90@gmail.com
Studieorter
-
-
-
Sakarya, Turkiet (Türkiye)
- Sakarya University-Anesthesiology and Reanimation Department
-
Kontakt:
- Burçin Alaçam
- Telefonnummer: +905465903851
- E-post: burcin.ersoy90@gmail.com
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Testmetod
Studera befolkning
Beskrivning
Inclusion Criteria:
- Patients undergoing elective upper extremity hand surgery
- 18 - 65 years
- ASA I
- No coagulopathy, thrombocytopenia, coagulation disorders
- Patients who provide informed consent to participate in the study
Exclusion Criteria:
- History of drug allergy relevant to study procedures or local anesthetics
- Body mass index (BMI) ≥ 30 kg/m²
- Body weight < 40 kg
- Age < 18 years or > 65 years
- History of significant cardiac disease (e.g., arrhythmia, conduction abnormalities)
- Coagulopathy (INR > 1.5 or platelet count < 100,000/mm³)
- Pregnancy or lactation
- Infection at the site of peripheral nerve block
- ASA II-IV
- Failed block or motor block duration exceeding 30 minutes
- Patients reporting pain (NRS ≥ 3), due to potential influence on sympathetic activity
- Chronic opioid use
Studieplan
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
|---|---|
|
Infraclavicular Block Group
Patients undergoing routine ultrasound-guided infraclavicular brachial plexus block for upper extremity surgery will be included in this observational cohort.
Pulse Wave Transit Time (PWTT) and other hemodynamic parameters will be measured at predefined time points before and after block administration.
No additional intervention beyond standard clinical care will be performed for research purposes.
|
Ultrasound-guided infraclavicular brachial plexus block will be performed as part of routine clinical anesthesia practice for upper extremity surgery.
Local anesthetic will be administered according to standard institutional protocols.
No additional or experimental drug or procedure will be applied for research purposes.
Pulse Wave Transit Time (PWTT) and other hemodynamic parameters will be recorded before and after block placement at predefined time intervals.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Change in Pulse Wave Transit Time
Tidsram: 20 minutes after infraclavicular block
|
The primary outcome is the time-dependent change in Pulse Wave Transit Time (PWTT) following ultrasound-guided infraclavicular brachial plexus block.
PWTT will be measured as the interval between the R-wave of the electrocardiogram (ECG) and the corresponding pulse wave detected by peripheral pulse oximetry.
Measurements will be recorded at baseline (pre-block) and at 0, 5, 10, 15, and 20 minutes after block placement.
The primary analysis will evaluate the change in PWTT over time within the blocked extremity.
|
20 minutes after infraclavicular block
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Perfusion Index
Tidsram: 20 minutes after infraclavicular block
|
Changes in perfusion index (PI) measured from the pulse oximeter at the blocked and contralateral upper extremities at baseline and at 0, 5, 10, 15, and 20 minutes after infraclavicular block.
|
20 minutes after infraclavicular block
|
|
Skin Temperature
Tidsram: 20 minutes after infraclavicular block
|
Changes in skin temperature of the blocked and contralateral upper extremities measured at baseline and at 0, 5, 10, 15, and 20 minutes after block placement.
|
20 minutes after infraclavicular block
|
|
oxygen saturation
Tidsram: 20 minutes after infraclavicular block
|
Changes in peripheral oxygen saturation measured using pulse oximetry during the study period.
|
20 minutes after infraclavicular block
|
Samarbetspartners och utredare
Sponsor
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- SAU-ANE-BA-04
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .