Using Dermabond skin glue (DSG) on bridging leg incision instead of skin suture on the coronary artery bypass graft (CABG) leg donor site

ISRCTN	ISRCTN52787873
DOI	https://doi.org/10.1186/ISRCTN52787873
Secondary identifying numbers	N0226180190

Submission date: 28/09/2007
Registration date: 28/09/2007
Last edited: 12/04/2021

Recruitment status: No longer recruiting
Overall study status: Completed
Condition category: Surgery

Prospectively registered

Protocol

Statistical analysis plan

Results

Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Mrs Bhuvaneswari Bibleraaj
Scientific

University Hospital of South Manchester NHS Foundation Trust
Wythenshawe Hospital
Southmoor Road
Manchester
M23 9LT
United Kingdom

Phone	+44 (0)161 291 2078
Email	honey223@hotmail.com

Study information

Study design	Randomised controlled trial
Primary study design	Interventional
Secondary study design	Randomised controlled trial
Study setting(s)	Hospital
Study type	Treatment
Participant information sheet	Not available in web format, please use the contact details below to request a patient information sheet
Scientific title	Using Dermabond skin glue (DSG) on bridging leg incision instead of skin suture on the coronary artery bypass graft (CABG) leg donor site
Study objectives	To compare the use of Dermabond skin glue and skin suture on the CABG leg donor site.
Ethics approval(s)	Not provided at time of registration
Health condition(s) or problem(s) studied	Surgery: Coronary artery bypass grafting (CABG)
Intervention	1. Normal practice: usual bridging technique of harvesting long saphenous vein from the leg, and skin closure with 3/0 undyed stitch after subcutaneous layer 2. After normal subcutaneous layer closure, wound cleaned with dry swab and dermabond applied. Pressure bandage then applied.
Intervention type	Procedure/Surgery
Primary outcome measure	Healing of the leg wound, less infection rate, early rehabilitation, cosmetic effect of the scar, early discharge
Secondary outcome measures	No secondary outcome measures
Overall study start date	11/05/2006
Completion date	03/11/2006

Eligibility

Participant type(s)	Patient
Age group	Not Specified
Sex	Not Specified
Target number of participants	100
Total final enrolment	106
Key inclusion criteria	All elective patients undergoing coronary artery bypass grafting with all Consultants in Wythenshawe Hospital after patient permission.
Key exclusion criteria	1. Emergency coronary artery bypass grafting patients 2. Not currently taking part in another research project 3. Patients who do not want to participate in the study
Date of first enrolment	11/05/2006
Date of final enrolment	03/11/2006

Locations

Countries of recruitment

England
United Kingdom

Study participating centre

University Hospital of South Manchester NHS Foundation Trust

Manchester
M23 9LT
United Kingdom

Sponsor information

Record Provided by the NHSTCT Register - 2007 Update - Department of Health
Government

The Department of Health, Richmond House, 79 Whitehall
London
SW1A 2NL
United Kingdom

Phone	+44 (0)20 7307 2622
Email	dhmail@doh.gsi.org.uk
Website	http://www.dh.gov.uk/Home/fs/en

Funders

Funder type

Government

University Hospital of South Manchester NHS Foundation Trust (UK), NHS R&D Support Funding

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to share	No
IPD sharing plan summary	Not provided at time of registration
Publication and dissemination plan	Not provided at time of registration
IPD sharing plan

Study outputs

Output type	Details	Date created	Date added	Peer reviewed?	Patient-facing?
Results article		01/11/2009	12/04/2021	Yes	No

Editorial Notes

12/04/2021: The following changes have been made:
1. Publication reference added.
2. The final enrolment number has been added from the reference.
14/02/2020: No publications found, verifying study status with principal investigator.