Assistance of pain treatment through a continuous algesia-measurement for postoperative patients in the recovery room

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00000755

Enrollment

Registered

2011-04-11

Start date

2011-04-28

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 pain R52.9

Interventions

Group 1: Continously monitoring with Med-Storm Pain Monitor in addition to the periodic NRS questioning (each 15 min). An overstepping of the preset NFSC threshold value (correspondent to NRS of at le

Eligibility

Sex/Gender

All

Age

18 Years to 111 Years

Inclusion criteria

Inclusion criteria: at least 18 years competent surgical procedure, at least scheduled for 90 min. OP classification at least III general anaesthesia postoperative stay in the recovery room

Exclusion criteria

Exclusion criteria: beta blocker, ICD/ pacemaker, current catecholamines, epidural catheter, PCA pump

Design outcomes

Primary

Measure	Time frame
mean numeric rating score given by the patient	—

Secondary

Measure	Time frame
Number of pain events during the stay in the recovery room (RR), patient sastisfaction (questionaire after discharge of the RR), duration of stay in the RR, total dose of applicated analgetics (substance and dosis), incidence of side effects (nausea, vomitus, hypotension, hypertension, tachycardia, bradycardia), Aldrete score (each 15 min), salivatory cortisol level (at the beginning and the end of RR stay)	—

Measure

Time frame

Number of pain events during the stay in the recovery room (RR), patient sastisfaction (questionaire after discharge of the RR), duration of stay in the RR, total dose of applicated analgetics (substance and dosis), incidence of side effects (nausea, vomitus, hypotension, hypertension, tachycardia, bradycardia), Aldrete score (each 15 min), salivatory cortisol level (at the beginning and the end of RR stay)

—

Countries

Germany

Contacts

Public ContactMichael Czaplik

Universitätsklinikum Aachen Klinik für Anästhesiologie

mczaplik@ukaachen.de02418088179

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 25, 2026