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Reliability of continuous respiratory waveform monitoring in Thoracic Paravertebral Block

Reliability of continuous respiratory waveform monitoring in Thoracic Paravertebral Block: An observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20210208004
Enrollment
49
Registered
2021-02-08
Start date
2021-02-09
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

Significant severe kyphoscoliosis Coagulopathy Allergy to local anesthetic agents Pneumothorax Intrathecal anesthesia Epidural anesthesia

Interventions

Patients are undergoing to have thoracotomy or video-assisted thoracoscopy surgery under general anesthesia with ultrasound guided thoracic paravertebral block.
Diagnostic
Thoracic surgery patients

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Patient undergoing elective video-assisted thoracoscopic surgery and open thoracotomy for lung surgery with American Society of Anesthesiologists Classification 1-3

Exclusion criteria

Exclusion criteria: 1 Inability to obtain informed consent 2 Patients who refuse to receive thoracic paravertebral block 3 Body mass index > 35 kg/m2 4 Pre-existing neuropathy (assessed by history and physical examination) 5 History of previous thoracic surgery 6 Significant thoracic kyphoscoliosis 7 Coagulopathy (platelets < 100,000/mL or INR > 1.4) 8 Allergy or contraindicated to medications used in study protocol (Bupivacaine, sevoflurane, propofol, cisatracurium, fentanyl, morphine 9 Chronic pain syndromes requiring opioid intake at home 10 Active infectious condition 11 Refuse to participate or withdraw their consent at any stage of the study

Design outcomes

Primary

MeasureTime frame
Mean pressure and waveform immediately during the procedure and 1 hour after surgery Pressure value in mmHg

Secondary

MeasureTime frame
Analgesia level at PACU within 1 hour after finishing operation Sensory loss assessed by dermatome levels

Countries

Thailand

Contacts

Public ContactAmorn Vijitpavan

Faculty of Medicine Ramathibodi Hospital

fluotec@gmail.com0818191601

Outcome results

None listed

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