Skip to main content
MedPathMedPath Home
Clinical Trials/EUCTR2019-000515-84-BE
EUCTR2019-000515-84-BE
Active, not recruiting
Phase 1

Comparison of pain and comfort in patients following cardiac surgery: opioid-morphine managed vs multimodal pain-management. - MONDAY

Ghent University Hospital0 sites120 target enrollmentJuly 15, 2019
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
DrugsDexdor 100 microgram/ml concentraat voor oplossing voor infusieFentanyl-Janssen 0,05 mg/ml oplossing voor injectieKetalar 50 mg/ml, oplossing voor injectieLinisol 1 %, oplossing voor injectieLyrica 75 mg harde capsulesMAGNESIUM SULFATE STEROP 1g / 10ml Oplossing voor injectie

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Ghent University Hospital
Enrollment
120
Status
Active, not recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 15, 2019
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\- patients undergoing first time cardiac surgery by median sternotomy
  • •\- elective surgery or semi\-urgent: there needs to be time to provide 8 hours before surgery the intake of pregabalin
  • •\- \> or \= 18 years
  • •\- possibility to communicate with the patient to score pain and comfort
  • •\- signed informed consent, signed by subject able and willing to provide written informed consent for study participation
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range 60
  • •F.1\.3 Elderly (\>\=65 years) yes

Exclusion Criteria

  • •\- urgent surgery
  • •\- pregnancy and lactation
  • •\- hypersensitivity to any of the study medication
  • •\- in case of direct postoperative revision the patient is NOT excluded

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
Comparative study of pain levels following paediatric tonsillectomy using either conventional tonsillectomy instruments or the coblator device for tonsil removalSigns and Symptoms: PainSigns and SymptomsPain
ISRCTN07513663Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Completed
Not Applicable
Comparison of Pain experienced by patients in the recovery, after undergoing Laparoscopic surgeries, when placed flat on bed (supine position) and when the head end is elevated 30�° up( semi-fowlers position)
CTRI/2021/04/032812Aditya Gopal Sarma S66
Recruiting
Phase 3
morphine plus Naloxone in cesaria
IRCT20140524017811N8Sari University of Medical Sciences60
Suspended
Not Applicable
To evaluate the effectiveness of Low Level Lasers as pre anaesthetic agent
CTRI/2023/06/053739Dr Bollavaram Golla Aishwarya
Not yet recruiting
Not Applicable
To evaluate the effect of clove oil, betel leaf extract, lignocaine gels and ice for pain reduction during intraoral injections
CTRI/2020/12/029937Dr Kanchan M Tuppadmath