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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01866787
Other study ID # RH-4074-OJ3
Secondary ID
Status Recruiting
Phase N/A
First received February 4, 2013
Last updated January 15, 2015
Start date January 2013
Est. completion date December 2015

Study information

Verified date January 2015
Source Rigshospitalet, Denmark
Contact Øivind Jans, M.D
Email oeivind.jans@regionh.dk
Is FDA regulated No
Health authority Denmark: Danish Dataprotection Agency
Study type Observational

Clinical Trial Summary

The purpose of this observational study is to evaluate the baroreceptor function in relation to surgical inflammation and orthostatic intolerance after elective hip arthroplasty.

The main hypothesis is that baroreceptor function is attenuated after surgery and related to surgical inflammation.


Description:

Orthostatic intolerance and hypotension is prevalent during early mobilization after major surgery.

This observational study aims to evaluate the baroreceptor function during using a standardized evaluation protocol before, 6- and 24 hours after elective primary unilateral hip-arthroplasty.

The study hypothesis is that baroreceptor function as expressed by the valsalva ratio is attenuated after surgery and related to surgical inflammation.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Scheduled for unilateral hip arthroplasty

- 18 years or older

- Able to give informed consent

Exclusion Criteria:

- American Society of Anesthesiologists (ASA) class 3 or higher

- Chronic arrythmia (Atrial fibrillation or other arrythmia)

- Incompensated ischaemic heart disease

- Mobilization restriction due to surgical reasons

- Medical complications during admission requiring transferral to other department

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
Denmark Frederiksberg Hospital, Department of orthopaedic surgery Frederiksberg

Sponsors (2)

Lead Sponsor Collaborator
Rigshospitalet, Denmark Lundbeck Foundation

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in baroreceptor function from preoperatively to 6 hours after surgery Change in baroreceptor function as expressed by change in the blood pressure valsalva ratio during a standardized assessment before and 6 hours after surgery. 6 hours after surgery No
Secondary Orthostatic response in blood pressure The response in systolic and diastolic blood pressure during postural change from supine to standing Preoperative, 6 and 24 hours after surgery No
Secondary Orthostatic response in heart rate variability Heart rate variability during supine rest, sitting and standing as assessed by Spectral analysis. preoperative, 6 and 24 hours postoperative No
Secondary Orthostatic intolerance Orthostatic intolerance defined as the inability to sit or stand for 3 minutes due to presyncopal symptoms (Dizziness, Nausea, Blurred vision). preoperative, 6 and 24 hours after surgery No
Secondary Inflammatory markers Inflammatory markers (CRP and interleukin-6) measured at 3 separate timepoint: preoperative, 6- and 24 h after surgery preoperative, 6 and 24 hours postoperative No
Secondary Orthostatic Hypotension orthostatic hypotension defined according to international guidelines. Preoperative, 6 and 24 hours postoperative. No
Secondary Baroreceptor function baroreceptor function as expressed by change in the blood pressure valsalva ratio during a standardized assessment On the day of surgery: preoperatively, 6- and 24 hours after surgery No
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