MedPath

An assessment of the effects of pressors on graft blood flow after free tissue transfer surgery: A randomised study – Part II - Free 4 Flow (2)

Phase 1
Conditions
Patients in need of free flap facial reconstructive surgery
Registration Number
EUCTR2009-015533-79-GB
Lead Sponsor
Oxford Radcliffe Hospitals NHS Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Not specified
Target Recruitment
25
Inclusion Criteria

•Participant is willing and able to give informed consent for participation in the study.
•Male or Female, aged 18 years or above.
•Undergoing free flap surgery, with planned overnight ventilation on the Intensive Care Unit
•Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the study.

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
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

The participant may not enter the study if ANY of the following apply:
•Female participants who is pregnant, lactating
•Patients withholding consent
•Patients in whom pressor agents are contraindicated
•Patients who weigh more than 100kg
•Patients in whom overnight ventilation is not planned
•Patients having repeat surgery within four weeks of the original procedure and trial participation

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath