Patient satisfaction with different methods of analgosedation for dressing changes in burn patients

Patient satisfaction with different methods of analgosedation for dressing changes in burn patients - PAVAB

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00036125

Enrollment

Registered

2025-02-10

Start date

2025-03-03

Completion date

Unknown

Last updated

2026-04-27

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

Conditions

T30.0

Interventions

Group 1: Dressing changes after burns during the inpatient stay are performed with Ketamine/ Midazolam. Patient satisfaction with analgosedation and possible complications are recorded. Opioid consump

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: burn injury > 3 % und < 20 % total body surface area (TBSA)

Exclusion criteria

Exclusion criteria: Lack of consent to participate in the study Inpatient admission > 24 hours after burn injury pregnancy Primarily palliative therapy Chronic neuropathic pain syndrome Contraindications to any of the medications used for analgesic sedation

Design outcomes

Primary

Measure	Time frame
Patient satisfaction with the analgosedation procedure is surveyed at the time of discharge. The patient is asked to rate their satisfaction using a numerical rating scale from 10=highest satisfaction to 0=completely dissatisfied.	—

Secondary

Measure	Time frame
Consumption of Pregabalin and Opioids during hospital stay	—

Countries

Germany

Contacts

Public ContactJochen Gille

Klinikum St. Georg Leipzig gGmbH

Jochen.Gille@sanktgeorg.de+493419094706

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026