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Influence of different catheter designs for distal sciatic nerve blockade on postoperative pain intensity- a randomised controlled trial

Influence of different catheter designs for distal sciatic nerve blockade on postoperative pain intensity- a randomised controlled trial - CathPopSci

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00020938
Enrollment
140
Registered
2020-04-08
Start date
2016-09-14
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

findings requiring surgery on the distal lower leg / ankle or foot

Interventions

Group 1: curl-catheter placement Group 2: conventional straight catheter placement

Sponsors

Klinik für Anästhesiologie und Intensivtherapie Universitätsklinikum Carl Gustav Carus Dresden
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: - patients' consent form - indication for the placement of a distal ischiadicus blockage in the context of a surgical Intervention - age between 18 and 75 years

Exclusion criteria

Exclusion criteria: - chronic pain - refusal of regional anaesthesia - intolerance or allergy to ropivacaine or oxycodone - neuromuscular diseases - BMI > 35 - Polyneuropathy or ipsilateral neuropathy - pre-existing opioid medication

Design outcomes

Primary

MeasureTime frame
postoperative pain intensity on the day of surgery and on three subsequent days by means of NRS recording twice a day

Secondary

MeasureTime frame
In addition, the position of the pain catheters is recorded by means of sonographic control immediately after the operation and once a day on the first three postoperative days. Further parameters such as additional consumption of painkillers, amount of local anaesthetics administered, assessment of the puncture site and potential side effects are documented once a day. Finally, the time of catheter removal and patient satisfaction with the procedure is recorded with an NRS of 0 (completely dissatisfied) to 10 (very satisfied).

Countries

Germany

Contacts

Public ContactRosa Nickl

Klinik für Anästhesiologie und Intensivtherapie Universitätsklinikum Carl Gustav Carus Dresden

rosa.nickl@uniklinikum-dresden.de0351-4580

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 18, 2026