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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02380820
Other study ID # LOCAL/2014/CEDMH-01
Secondary ID 2014-A01214-43
Status Active, not recruiting
Phase N/A
First received February 23, 2015
Last updated March 21, 2016
Start date June 2015
Est. completion date April 2016

Study information

Verified date March 2016
Source Centre Hospitalier Universitaire de Nimes
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santéFrance: Committee for the Protection of Personnes
Study type Interventional

Clinical Trial Summary

The main objective of this study is to compare the Softform Premier mattress (in static mode) and AIRSOFT DUO mattresses in terms of skin pressures measured at the sacral area.


Description:

The secondary objectives of the study are to compare the two devices in terms of:

A. contact surface. B. heel pressure. C. On the occurrence of pressure ulcers anywhere on the body at month 1. D. patient comfort after 1 month (visual analog scale ranging from 1 to 10).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date April 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- The patient must have given his/her informed and signed consent

- The patient must be insured or beneficiary of a health insurance plan

- The patient spends more than 12 hours in bed with a possible verticalization and a predictable length of stay of at least 1 month.

- The patient has a stable medical condition (no complications in the last 10 days) without pressure ulcers

- The patient is at risk of pressure ulcers assessed a score = 14 on the Norton scale

- The patient's weight is less than 120 Kg

Exclusion Criteria:

- The patient is in an exclusion period determined by a previous study

- The patient is under judicial protection, under tutorship or curatorship

- The patient refuses to sign the consent

- It is impossible to correctly inform the patient

- Contra-indication for strict decubitus dorsal position

- The patient has a rotation of the pelvis, asymmetric deformations of the hips in the frontal plane.

- The patient has bedsores, a recent scar in a pressure area.

- The patient has a knee flexion deformity> 10 °

- The patient is agitated or uncooperative

- The patient's weight is greater than 120 Kg

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Device:
Airsoft Duo mattress
A multi-layer mattress for pressure sore prevention. Made by NAUER FOAMPARTNER AG et OBA AG (Germany).
Softform Premier mattress (in static mode)
A multi-layer mattress for pressure sore prevention. Made by INVACARE MSS (United Kingdom).

Locations

Country Name City State
France EHPAD La Chimotaie Cugan Montaigu Cedex
France CHRU de Nîmes - Hôpital Universitaire Carémeau Nîmes Cedex 09
France EHPAD Notre Dame des Pins Saint Privat des Vieux

Sponsors (2)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nimes Invacare Poirier S.A.S.

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Other Age (years) Baseline (Day 0) No
Other Sex (F/M) Baseline (Day 0) No
Other Weight (kg) Baseline (Day 0) No
Other Height (cm) Baseline (Day 0) No
Other Body mass index (kg/m^2) Baseline (Day 0) No
Other Norton risk score Baseline (Day 0) No
Other Albuminemia Baseline (Day 0) No
Primary Interface pressure in the sacral zone (mm Hg) as measured by a Model X3 sensor pressure captor sheet Day 1 No
Secondary Contact surface area (cm^2) as measured by a Model X3 sensor pressure captor sheet Day 1 No
Secondary Interface pressure at the heel (mm Hg) as measured by a Model X3 sensor pressure captor sheet Day 1 No
Secondary Presence/absence of a pressure ulcer over the past month 1 month No
Secondary Patient-rated comfort as measured by the visual analog scale Visual analog scale ranging from 0 to 10 1 month No
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