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Effect of programmed intermittent paravertebral bolus analgesia on perioperative neurocognitive recovery in elderly patients undergoing VATS

Effect of programmed intermittent paravertebral bolus analgesia on perioperative neurocognitive recovery in elderly patients undergoing VATS

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061670
Enrollment
Unknown
Registered
2022-06-30
Start date
2022-06-30
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Perioperative neurocognitive dysfunction

Interventions

Program controlled paravertebral analgesic group:Preoperative paravertebral catheterization and 20mL injection of 0.5% ropivacaine solution from the catheter, postoperative program-controlled paravert
Intravenous patient controlled analgesia group:Postoperative intravenous patient controlled analgesia

Sponsors

Beijing Chest Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 60 - 75 years, no gender limitation; 2. Patients with clear consciousness and good communication; 3. Pulmonary resection with VATS was performed.

Exclusion criteria

Exclusion criteria: 1. Refused or failed to complete preoperative cognitive function tests; 2. Dementia, or central nervous system diseases that may lead to dementia, such as cerebrovascular disease, Parkinson's disease, encephalitis, epilepsy, brain tumors, brain trauma, etc.; 3. MMSE score < 24; 4. preoperative hearing or vision impairment, communication difficulties; 5. Serious sleep disorders, long-term use of sedatives, antidepressants or alcohol; 6. Patients with persistent chronic pain or long-term oral opioid analgesics before surgery; 7. Patients undergoing thoracotomy or serious surgical complications requiring a second operation.

Design outcomes

Primary

MeasureTime frame
Incidence of delayed early cognitive recovery;

Secondary

MeasureTime frame
number rating score;The Montreal Cognitive Assessment Scores;Montreal Cognitive assessment scores (telephone type);Mean arterial pressure;Total opioid consumption within (including analgesic pump dosage and analgesic relief opioid dosage);Postoperative delirium;postoperative nausea and vomiting;Postoperative chronic pain;Neurofilament light protein;tau protein;IL-6;tumor necrosis factor-a;C-Reactive Protein;Duration of chest tube indwelling;analgesic remedy;15-item recovery quality rating scale score;Neuropathic pain Scale;

Countries

China

Contacts

Public ContactLiu Wei

Beijing Tuberculosis and Thoracic Tumor Research Institute

lw1200@sina.com+86 13621153330

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 25, 2026