QUIPS - Quality improvement in post operative pain treatment

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00006153

Enrollment

1000000

Registered

2014-05-12

Start date

2004-08-02

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

R52.0

Interventions

Group 1: On postop day 1, patients are asked about their pain/their assessment of the pain therapy

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patient consents to participate, - patient is post-op day 1, - patients speaks German, patient is able to fill in the questionnaire

Exclusion criteria

Exclusion criteria: - patient refuses participation - patient doesn't speak German - patient is not post-op day 1 - patient is not able to fill in the questionnaire (sedated, confused, fast asleep)

Design outcomes

Primary

Measure	Time frame
Outcome quality in postoperative pain therapy, assessed by the parameters pain intensity and side effects. Patient reported outcomes. Questionnaire filled in on postop day 1.	—

Secondary

Measure	Time frame
Patient satisfaction, process- and structure parameters of postoperative pain therapy (e.g. pain measurement, adequate medication, involving patients)	—

Countries

Austria, Germany, Luxembourg

Contacts

Public ContactClaudia Weinmann

Universitätsklinikum Jena Klinik für Anästhesiologie und Intensivmedizin

claudia.weinmann@med.uni-jena.de03641 9323398

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 5, 2026