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Evaluation of pain-relevant outcomes after ambulatory surgery – AQS1

Evaluation of pain-relevant outcomes after ambulatory surgery – AQS1 - SAMBA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00028052
Enrollment
100000
Registered
2022-02-08
Start date
2001-07-01
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

ambulatory surgery

Interventions

Group 1: Patients operated in AQS1-participating practices and clinics in Germany. Data basis is the patient information and information from the physician section of the AQA1 (see details under prim

Sponsors

Leiter Fachbereich SchmerztherapieKlinik für Anästhesiologie und IntensivmedizinUniversitätsklinikum Jena
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Operation in the period 01.01.2004 - 31.12.2021 age >= 18 years

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
Complaints due to wound pain until day 3 after surgery.

Secondary

MeasureTime frame
Additional variables from the patient section of the AQS1: o adequate supply of pain medication in the recovery room o effects of head, throat and muscular pain after surgery o effect of wound pain after day 3 after surgery o adequate supply of pain medication at home o overall rating of the surgery Data from the physician section of the AQS1: complaints in the recovery room (wound, muscle, neck, and head pain). In addition, there is a detailed presentation of demographic (e.g., age, gender, ASA) and procedure-associated variables (type of anesthesia, medication, duration of surgery) as well as postoperative complications.

Countries

Germany

Contacts

Public ContactPhilipp Baumbach

Klinik für Anästhesiologie und IntensivmedizinUniversitätsklinikum Jena

Philipp.Baumbach@med.uni-jena.de+49-3641-9-325798

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 9, 2026