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Evaluation of Perineural Catheterization Practices in Postoperative Orthopedic Surgery

Evaluation of Perineural Catheterization Practices in Postoperative Orthopedic Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04011839
Acronym
Cathepos
Enrollment
7
Registered
2019-07-09
Start date
2021-06-07
Completion date
2022-06-29
Last updated
2025-05-30

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

Conditions

Analgesia

Brief summary

Continuous peripheral nerve blocks are considered as the gold standard for postoperative analgesia in orthopaedic surgery (shoulder, knee, foot). These techniques are also used in chronic pain. The main disadvantage of these techniques is that they can drive a more or less deep motor block that slows down the rehabilitation process. This disadvantage could be prevented (or minimized) by adapting the protocol for administering local anesthetics or by changing molecules (levobupivacaine 0.625 mg/ml instead of ropivacaine 2 mg/ml). There is no literature comparing the effectiveness of the sensory block and its impact on the motor block according to the administration protocol and/or the type of local anesthetics. The main judgement criterion of such a study could be a composite criterion crossing the quality of the sensory block and the depth of the motor blockades, the ideal being to have a perfect sensory block without any motor block.

Interventions

Use of Levobupivacaïne instead ropivacaïne

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \>18 years old * ASA score 1 to 4 * Scheduled orthopaedic surgery * consent to participate

Exclusion criteria

* Pregnant, parturient, or breastfeeding woman * Emergency situation * Contraindications to local anaesthesia * Patient refusal

Design outcomes

Primary

MeasureTime frameDescription
Comparison between sensory Block Quality and motor Block deepDay1 to Day 3Composite score between 0 to 2 for Sensory Block and 0 to 2 for motor Block

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026