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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04952649
Other study ID # PITCH
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 7, 2021
Est. completion date December 30, 2022

Study information

Verified date July 2021
Source Shanghai Zhongshan Hospital
Contact Guo-wei Tu, MD PhD
Phone 13501996995
Email tu.guowei@zs-hospital.sh.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pacemakers are widely used in postcardiotomy patients to avoid severe arrhythmia. The peripheral perfusion index (PI) has been considered as an effective parameter evaluating the circulation. In this study, investigators aim to avaluate the ability of peripheral perfusion index to detect changes of hemodynamics in postcardiotomy patients with pacemakers.


Description:

Pacemakers are widely used in postcardiotomy patients to avoid severe arrhythmia. The peripheral perfusion index (PI) has been considered as an effective parameter evaluating the circulation. In this study, investigators aim to evaluate the ability of peripheral perfusion index to detect changes of hemodynamics (cardiac output or storke volume,et al) in postcardiotomy patients with pacemakers.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 30, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - age >=18 years old; - postcardiotomy - placement of temportary pacemaker during the surgery - dependence of pacemaker (abscence of autonomic cardiac rhythm) Exclusion Criteria: - hemodynamic unstable (high dose of vasoactive drugs) - fingers ischemia, cannot monitor the peripheral perfusion index

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Zhongshan Hospital, Fudan University Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital

Country where clinical trial is conducted

China, 

References & Publications (2)

Abdel-Ghaffar HS, Abdel-Wahab AH, Roushdy MM. Using the perfusion index to predict changes in the depth of anesthesia in children compared with the A-line Autoregression Index: an observational study. Braz J Anesthesiol. 2021 May 12. pii: S0104-0014(21)00198-6. doi: 10.1016/j.bjane.2021.04.030. [Epub ahead of print] — View Citation

Bazaraa H, Roby S, Salah E, Algebaly H. Assessment of Tissue Perfusion Using the Peripheral Perfusion Index and Lactate Clearance in Shock in Pediatric Patients. Shock. 2021 May 19. doi: 10.1097/SHK.0000000000001811. [Epub ahead of print] — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Cardiac output Measurement of cardiac output by Flotrac ,the metric is L/min. During the study procedure
Primary stroke volume Measurement of stroke volume by Flotrac ,the metric is ml. During the study procedure
Primary Peripheral perfusion index Measurement of Peripheral perfusion index by masimo radical. During the study procedure
See also
  Status Clinical Trial Phase
Completed NCT00182416 - Second Canadian Trial of Physiologic Pacing (CTOPP II): Pilot Trial Phase 3