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Effect of Forced-air Warming and Circulating-water Mattress in Preventing Heat Loss During Vascular Surgery

M

Mahidol University

Status and phase

Completed
Phase 2

Conditions

Forced-air Warming Mattress
Vascular Surgery
Hypothermia
Circulating-water Mattress

Treatments

Device: warming device (a reusable, custom-made forced- air warming mattress)

Study type

Interventional

Funder types

Other

Identifiers

NCT00712023
Si 196/2007
003(1)/50

Details and patient eligibility

About

The purpose of this study is to determine whether a custom-made forced-air warming mattress can prevent heat loss in patients undergoing vascular surgery better than a circulating-water mattress

Full description

A reusable, custom-made forced-air warming mattress was made of a light to medium weight water resistant canvas, sewn like mattress with 2 arms placed underneath the patient. An open hole at proximal part of one arm was designed to attach with a hose of warm air delivery device. Small holes (2-3 mm2), 5 inches apart were punched on the upper surface of this mattress around the patient except for the area underneath the patient that the holes were 9 inches apart. The weight of the patient will obstruct the air flow and prevent direct blowing of warm air onto the underside of patients. There is a special appendage connected to the upper part of mattress which can connect warm air to cover the patient's chest. There is a special appendage connected to the upper part of mattress which can convect warm air to cover the patient's chest. The mattress is 97 inches x 97 inches, with 2 arms of 25 inches x 16 inches and a special appendage of 45 inches x 12 inches for covering the chest with warm air delivery. This size is proper for patient of 170 cm. height. In order to reuse it, the mattress can be washed, dried and sterilized by gas or autoclaved for more than 50 times. A sterile sheet well enhance the sterile environment of the operating field.

Enrollment

44 patients

Sex

All

Ages

20 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients undergoing vascular surgery

Exclusion criteria

Preoperative fever

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

44 participants in 2 patient groups

1
Active Comparator group
Description:
warming by circulating-water mattress
Treatment:
Device: warming device (a reusable, custom-made forced- air warming mattress)
2
No Intervention group
Description:
Forced-air warming mattress

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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