Effectivity of a standardized, protocol-based, postoperative visit to verify the effectiveness of a clinic-wide used postoperative acute pain standard.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00025895

Enrollment

3500

Registered

2021-09-08

Start date

2021-11-01

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

postoperative acute pain R52 R52.0

Interventions

Group 1: Post-operative patients will be surveyed once about their quality of life and pain using the questionnaires "Post-anesthesiological Evaluation" and a questionnaire designed for this study.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: postoperative, inpatient patients

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

Measure	Time frame
The aim of the study "Effectiveness of a standardized, protocol-based, postoperative visit to check the effectiveness of a clinic-wide postoperative pain standard" is to check the significance of the "Post-anesthesiological evaluation" regarding postoperative pain.	—

Secondary

Measure	Time frame
To exam the patient satisfaction regarding anesthesiological care.	—

Countries

Germany

Contacts

Public ContactDietrich Henzler

Universitätsklinik für Anästhesiologie, operative Intensivmedizin, Rettungsmedizin, Schmerztherapie, Campus OWL, Klinikum Herford AöR

dietrich.henzler@klinikum-herford.de+49 (0)5221 94 2481

Outcome results

None listed

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