Intercostal catheter for analgesia post minimally invasive mitral valve surgery: A randomised, double blind study.

Not Applicable

• Conditions: Analgesia post minimally invasive mitral valve surgery; I34.0; Mitral (valve) insufficiency

• Registration Number: DRKS00015650
• Lead Sponsor: niversitätsklinikum Ulm, Sektion Kardioanästhesiologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2016-12-11
• Study Start: 2018-10-04
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 104

Inclusion Criteria

Minimally invasive mitral valve surgery.

Exclusion Criteria

Allergy against the medication put to use; ongoing use of antidepressants, antipsychotics, and analgetics; unability to use the VAS score.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Piritramid consumption during 8 hours postoperatively. The aim ist a score of 3 or below on the VAS; responsible for interviewing the Patient are the nursing staff.

Secondary Outcome Measures

Name	Time	Method
Ventilator time, Hospital time, Maximum VAS scores.