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Randomised comparison of inpatient pain management for sled prostheses

Randomised comparison of inpatient pain management for sled prostheses

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00029340
Enrollment
70
Registered
2022-07-05
Start date
2021-10-19
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

M17.1

Interventions

Group 1: LIA injection: Preoperatively, a baseline value for the functionality of the knee joint to be operated on is recorded by means of WOMAC, OKS and KOOS and the patients general state of health

Sponsors

Medizinische Hochschule Hannover
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: - Indication for primary sled prosthesis implantation - Age: 18 - 85 years

Exclusion criteria

Exclusion criteria: - Known diseases of the cardiovascular system that lead to severe limitations in exercise capacity, corresponding to NYHA3 and NYHA4. - Known dementia - Known drug abuse - Intolerances and/or allergies that make participation in the study impossible.

Design outcomes

Primary

MeasureTime frame
Assessment of knee joint function by torque measurement after 6 weeks postoperatively to record the quadriceps femoris muscle function of the 2 study groups with different analgesia regimens (LIA group, NKF group).

Secondary

MeasureTime frame
- Analgesic/opioid consumption - Side effects of analgesics - Complications - Patient satisfaction - Length of hospital stay - Assessment of chronic pain status

Countries

Germany

Contacts

Public ContactYvonne Noll

Orthopädische Klinik der Medizinischen Hochschule Hannover im Diakovere Annastift, Leitung Klinisches Studienmanagement

yvonne.noll@diakovere.de0511-5354-649

Outcome results

None listed

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