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Magen Haim Project - Assessing Hand Hygiene Formulas

S

Sheba Medical Center

Status and phase

Unknown
Phase 4

Conditions

Comparing Use of Hand Hygiene Products

Treatments

Other: Septol
Other: AniosGel 85 NPC
Other: Softa-Man (Braun)

Study type

Interventional

Funder types

Other

Identifiers

NCT03188549
SHEBA-17-3882-GR-CTIL

Details and patient eligibility

About

Background: Procedures of hand hygiene are an important component in prevention of cross-transmission of infections in hospitals. In recent years, hand washing with antiseptic soap (chlorhexidine) was replaced with use of alcohol-based hand rub. This change brought an increase in compliance with hand hygiene regulations from 30-40% to over 50%, and in other places up to 70%. However, even 70% compliance is not enough. One of the reported reasons for lack of compliance of staff to the use of alcohol-based preparations is skin irritation and dryness of the hands as a result of frequent use. At Sheba, like the majority of Israeli hospitals, the product used for handwashing is Septol (Teva), which includes 0.5% chlorhexidine gluconate (CHG) and 70% ethyl alcohol. The CDC, WHO and FDA guidelines approve for use of hospital hand hygiene, products that contain between 61-85% ethanol.

The investigators will replace the Septol currently used with a different alcohol-based antiseptic that is more user-friendly, and aim to determine whether this will increase the compliance with hand hygiene protocols.

The investigators will assess

  1. Satisfaction of staff.
  2. Increase of hand hygiene compliance.

Full description

RESEARCH PATTERN:

Comparative research, Cross-Over, with a quasi-experimental component, comparing trial products to the use of Septol over the course of the year before the research.

Included in the study will be 29 departments of Sheba, whilst the other hospital departments will serve as a control group. The 29 departments will be divided into two branches with similar departments in each (each branch consisting of 3 internal medicine departments, 3 urgent care departments, a pediatric department, a surgical department, etc.). In Stage I (the initial six months), Branch A will exchange Septol with AniosGel, and Branch B will exchange Septol with Softa-Man. In Stage II (the second six months), Branch A will change to Softa-Man and Branch B will change to AniosGel. Branch C will be the control, where Septol will be used throughout the duration of the study.

STUDY POPULATION:

For objectives 1 and 2: All medical staff at Sheba (in all 3 branches of the study).

Total: 15 Departments in Branch A, 14 Departments in Branch B

Stages of the Study:

  1. At point zero (while still using Septol), distribute a questionnaire of hand hygiene compliance and satisfaction.
  2. Instruction to Branch A and Branch B departments regarding the switch of Septol to the new product (instruction to staff in all sectors of these departments).
  3. Exchange antiseptic Septol with the trial product in departments of Branch A and Branch B for the first six months (Stage I).
  4. At point one (six months into the study), distribute a questionnaire of hand hygiene compliance and satisfaction.
  5. Interim analysis of the questionnaires from point zero and point one.
  6. Instruction to departments regarding the switch of products, regarding the use of the new product.
  7. Exchange of trial product between the two groups for the second six month period (Stage II).
  8. At point two (twelve months into the study), distribute a questionnaire of hand hygiene compliance and satisfaction.
  9. Final analysis of questionnaires from Point 0, 1, and 2, as well as compliance of hand hygiene.

Enrollment

1,505 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All staff in the participating departments

Exclusion criteria

  • No

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

1,505 participants in 3 patient groups

Departments of Branch A
Active Comparator group
Description:
Intervention: AniosGel Respiratory ICU Pediatric Cardiac Surgery, NICU Hemato-Oncology, Oncology Internal A, C, D, E, F Surgery C, Vascular Surgery and Chest Surgery Pediatric B South Imaging Orthopedics B
Treatment:
Other: AniosGel 85 NPC
Departments of Branch B
Active Comparator group
Description:
Intervention: Softaman Neurosurgery ICU Cardiac Surgery, Cardiac ICU, Pediatric ICU Pediatric Hemato-Oncology Internal B and I, Geriatric C and D Surgery B Pediatric B North Emergency Room Orthopedics A and Hand
Treatment:
Other: Softa-Man (Braun)
Branch C
Active Comparator group
Description:
Control Intervention - Septol without any changes All patients hospitalized in the 29 departments in Sheba, including two of the branches, during the year of the study
Treatment:
Other: Septol

Trial contacts and locations

1

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Central trial contact

Ilana Tal, Nurse; Gili Regev-Yochay, MD

Data sourced from clinicaltrials.gov

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