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Paravertebral versus systemic Analgesia for video-assisted Lobectomy

Paravertebral versus systemic Analgesia for video-assisted Lobectomy - VATSLOPAIN

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00007529
Enrollment
160
Registered
2015-06-10
Start date
2015-04-07
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

C34

Interventions

Group 1: regional Anethesia using thoracic paravertebral analgesia, Ropivacain 0,2% with flow rate 8 ml/h, retrospective data collection Group 2: iv Opioid, PCA with application of Piritramide, bolus

Sponsors

Universitätsklinikum Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: • Inclusion criteria: Sex: male/female; Age: 18 – 75 years; informed consent of the patient; elective VATS lobectomy; Lobectomy between 01.01.2014 and 01.01.2015

Exclusion criteria

Exclusion criteria: • Exclusion criteria: switch to open thoracotomy resection; contraindications against the use of regional techniques: known allergy to local anaesthetics; infection around the puncture site; coagulation disorders; Scoliosis; drug abuse; emergency surgery; pregnancy. Language barrier; death

Design outcomes

Primary

MeasureTime frame
postoperative pain using visual analog scale 4h, 8h, 16h, 24h, 48h and 72h postoperative

Secondary

MeasureTime frame
Respiratory adverse events Spirometry at discharge Duration of hospital stay

Countries

Germany

Contacts

Public ContactBenedikt Haager

Universitätsklinikum Freiburg

benedikt.haager@uniklinik-freiburg.de0761-27024010

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 20, 2026