Skip to content

Intrapleural analgesy Catheter vs SAPB Catheter at ventral anterior spine surgery

Intrapleural analgesy Catheter vs SAPB Catheter at ventral anterior spine surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00035730
Enrollment
56
Registered
2025-04-01
Start date
2024-04-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Difference in opioid consumption in ventral thoracic spine surgery

Interventions

Group 1: Regional anesthesia with a serratus anterior plane block using the catheter technique Group 2: Regional anesthesia with Pleural pain catheter

Sponsors

BG Unfallklinik Frankfurt am Main
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Mono- or bisegmental ventral thoracic vertebral body replacement at level BWK10 to LWK2

Exclusion criteria

Exclusion criteria: Patient refusal, unconsciousness, chronic opioid use, BMI over 40, ASA 4-5 patients, non-consenting patients, known allergy to local anesthetics of the amide type, infection in the puncture area and patients who are unable to communicate adequately using available communication methods

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the difference in opioid consumption in relation to morphine within the first three days after insertion of the pain catheters.

Secondary

MeasureTime frame
-The clinical parameters should be recorded on the day of surgery, as well as other pain areas at the specified times: initially postoperatively (in the recovery room), then on days 1, 2 and 3 and as part of the postoperative follow-up examination after approximately 90 days. -assessment of PIC score -Lung function test -mobilization score -Anesthesia quality/ analgesia quality

Countries

Germany

Contacts

Public ContactFlorian Nikesch

BG Unfallklinik Frankfurt am Main

florian.nikesch@bgu-frankfurt.de+49 69 4753048

Outcome results

None listed

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