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Parascapular sub-iliocostalis Plane in Analgesia for Thoracoscopic Surgery

Parascapular sub-iliocostalis Plane in Analgesia for Thoracoscopic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117201
Enrollment
Unknown
Registered
2026-01-21
Start date
2026-01-21
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

None

Interventions

RISS block group:Before the surgery, perform ultrasound-guided RISS block on the patient
PSIP block group:Before the surgery, perform ultrasound-guided PSIP block on the patient
Vascular analgesia group:Intravenous analgesics are used for pain relief only after surgery

Sponsors

Ningbo Medical Centre Lihuili Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age 18~75 years old; 2.Scheduled for elective thoracoscopic surgery (such as lobectomy, segmentectomy, mediastinal tumor resection, etc.); 3.ASA classification grade I~III; 4.Sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Allergic to local anesthetics; 2.Coagulation dysfunction (INR > 1.5 or platelets < 50×10?/L); 3.Puncture site infection or anatomical abnormality; 4.Long-term use of opioids or analgesic medications; 5.Unable to cooperate with postoperative pain assessment;

Design outcomes

Primary

MeasureTime frame
VAS score within 24 hours postoperatively;

Secondary

MeasureTime frame
Time to first postoperative analgesic requirement;Restore Quality Score;Blockage-related complications;Analgesic drug usage within 48 hours postoperatively;Patient satisfaction score;Incidence of postoperative complications;

Countries

China

Contacts

Public ContactPing Li

Ningbo Medical Center Liweili Hospital

liping158581@163.com+86 574 5583 5583

Outcome results

None listed

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