Bernese Next of Kin Survey Following Organ Donation Request

• Sponsor: University Hospital Inselspital, Berne (Other)
• Overall Status: Completed
• CT.gov ID: NCT03612024
• Collaborator: (none)
• Enrollment: 117
• Location: 1
• Actual Duration (Months): 4.8
• Patients Per Site Per Month: 24.6

Study Details

Study Description

Brief Summary

6 to 18 months after organ donation request a next of kin survey using a standardized questionnaire was conducted.

Condition or Disease	Intervention/Treatment	Phase
Organ Donation; Next of Kin; Post Traumatic Stress Disorder	Behavioral: questionnaire

Study Design

• Study Type: Observational
• Actual Enrollment: 117 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Next of Kin Survey Following Organ Donation Request - a Single Center Experience
• Actual Study Start Date: Mar 1, 2018
• Actual Primary Completion Date: Jul 1, 2018
• Actual Study Completion Date: Jul 24, 2018

Arms and Interventions

Arm	Intervention/Treatment
request for organ donation approved	Behavioral: questionnaire; a standardized questionnaire was sent to all participants
request for organ donation rejected	Behavioral: questionnaire; a standardized questionnaire was sent to all participants

Outcome Measures

Primary Outcome Measures

1. factors influencing approval/rejection of an organ donation [6 to 18 months pre questionnaire]

2. factors with influence on mourning porcess [6 to 18 months past request]

Eligibility Criteria

Criteria

• Ages Eligible for Study: N/A and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

Next of kin involved in request for organ donation

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Department for Intensive Care Medicine	Bern		Switzerland	3010

Sponsors and Collaborators

• University Hospital Inselspital, Berne

Investigators

• Principal Investigator: Andreas Bloch, MD, department of critical care medicine, inselspital, university hospital, bern, university of bern

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Andreas Bloch, Andreas Bloch, MD, Concultant Intensive Care Medicine, University Hospital Inselspital, Berne
• ClinicalTrials.gov Identifier: NCT03612024
• Other Study ID Numbers: BNoKSurvey FODR
• First Posted: Aug 2, 2018
• Last Update Posted: Aug 31, 2018
• Last Verified: Aug 1, 2018

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Stress Disorders, Traumatic; Stress Disorders, Post-Traumatic

Study Results

No Results Posted as of Aug 31, 2018