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A Randomized trial of performance of continuous finger cuff blood pressure monitoring with HPI guided versus oscillometric blood pressure monitoring in open thoracic surgery : pilot study

A Randomized trial of performance of continuous finger cuff blood pressure monitoring with HPI guided versus oscillometric blood pressure monitoring in open thoracic surgery : pilot study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240721001
Enrollment
40
Registered
2024-07-21
Start date
2024-08-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Open thoracotomy Continuous finger cuff blood pressure monitoring, hemodynamic monitoring, Intraoperative hypotension, hypotension prediction, oscillometric blood pressure monitoring

Interventions

Anesthesiologist get information both from continous fingercuff blood pressure monitoring with HPI and hemodynamic parameters and conventional oscillometric blood pressure monitoring,Anesthesiologist
Experimental Device,No Intervention No treatment
Continous fingercuff blood pressure monitoring,Conventional oscillometric blood pressure monitoring

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years 2. American Society of Anesthesiologists Physical Status I, II 3. Elective surgery 4. Undergone general anesthesia 5. BMI between 18-35 kg/m2

Exclusion criteria

Exclusion criteria: 1. Bilateral thoracotomy 2. Emergency surgery 3. Require invasive intraarterial blood pressure monitoring 4. Underlying diseases : Peripheral arterial disease, Chronic kidney disease stage G3A or more, Aortic valvular disease 5. Combined with regional anesthesia or peripheral nerve block 6. Cognitive dysfunction 7. Pregnancy 8. Psychiatric diseases which can not judge to participate the study by themselves 9. Patients who can not complete the MoCA before surgery

Design outcomes

Primary

MeasureTime frame
time weighted average blood pressure lower than 65 mmHg during general anesthesia Data from continuous fingercuff blood pressure monitoring

Secondary

MeasureTime frame
acute kidney injury 24 hours after the end of anesthesia serum creatinine,postoperative derilium 24 hours after the end of anesthesia MoCA assessment

Countries

Thailand

Contacts

Public ContactSiree Dolnimitsakul

Faculty of Medicine, Chulalongkorn University

somwansiree@gmail.com0646459151

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026