Skip to content

Study on the effect of preoperative or postoperative thoracic paravertebral nerve block on the recovery quality of thoracic patients

Study on the effect of preoperative or postoperative thoracic paravertebral nerve block on the recovery quality of thoracic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092161
Enrollment
Unknown
Registered
2024-11-11
Start date
2024-11-11
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Pulmonary surgical diseases

Interventions

Treatment group:Perform TPVB before surgical skin incision
Control group:Perform TPVB after surgical suturing of the skin

Sponsors

Zigong Fourth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Accept elective VATS lobectomy or segmentectomy surgery, and routinely receive general anesthesia combined with thoracic paravertebral nerve block; 2. Age range: 18-65 years old; 3. ASA I-III level.

Exclusion criteria

Exclusion criteria: 1. Acute or chronic respiratory failure, chronic obstructive pulmonary disease GOLD grade = III, poor asthma control or acute respiratory distress syndrome patients; 2. Serious cardiovascular complications, such as NYHA = III, acute coronary syndrome, or persistent ventricular tachycardia; 3. Previous history of ipsilateral thoracic surgery or history of general anesthesia surgery under mechanical ventilation within one month prior to surgery; 4. Patients with contraindications for TPVB (coagulation dysfunction, anticoagulant or antiplatelet therapy, skin ulcer infection, local anesthetic allergy, spinal deformity, etc.); 5. Patients with tracheal malformation or difficulty in tracheal intubation; 6. Unable to provide written informed consent.

Design outcomes

Primary

MeasureTime frame
Postoperative 24-hour recovery quality score;Incidence of postoperative adverse reactions;

Secondary

MeasureTime frame
Postoperative 48-hour recovery quality score;Postoperative pain score;Postoperative opioid consumption;Time of first postoperative rescue analgesia;Postoperative incidence of pulmonary complications;

Countries

China

Contacts

Public ContactSong Jianli

Zigong Fourth People's Hospital

songjlxx@163.com+86 157 0049 0896

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026