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Surgeons' Satisfaction With Two Types of Tinted Chlorhexidine Applicators (Chloraprep® and Nex Clorex 2%)

Comparative Study to Asses the Satisfaction With Tinted Chlorhexidine Applicators (Chloraprep® and Nex Clorex 2%)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03508492
Enrollment
22
Registered
2018-04-25
Start date
2018-04-30
Completion date
2018-06-30
Last updated
2018-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Product Quality, Satisfaction

Brief summary

The development of surgical site infections (SSI) in clean-contaminated surgery is regarded as being preventable. Known to be effective in the prevention of surgical site infection are the adequate sterilization of the surgical instruments, asepsis during operation, antibiotic prophylaxis where indicated, and certainly the preparation of the skin at the incision site. During the last decades the use of alcoholic chlorhexidine has replaced povidone iodine for preoperative skin preparation. In order to improve the way alcoholic chlorhexidine is applied, pharmaceutical industry has developed new applicators. This randomized study was conducted to know the surgeons' satisfaction within the use of two tinted applicators: Chloraprep® and Nex Clorex 2%

Interventions

OTHERSurgical tinted Chloraprep® applicators

We randomized knee, hip, cardiac and colon surgeons making them using two applicators of each brand in four of theirs surgeries. Randomization will be carried out in blocks of four for each surgeon.

OTHERSurgical tinted Nex Clorex 2% applicators

We randomized knee, hip, cardiac and colon surgeons making them using two applicators of each brand in four of theirs surgeries. Randomization will be carried out in blocks of four for each surgeon.

Sponsors

Cristina Fernandez Perez
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Volunteer surgeons from colon, cardiac, knee and hip surgical departments. Once surgeon has enrolled the study, patients will be selected if they have hospital admission with scheduled surgery and have signed informed consent

Exclusion criteria

* Urgent surgeries * Outpatient surgery * Surgical complex cures * Mixed interventions: exploratory or sequential * Unscheduled surgeries * Rejection of participation * Chlorhexidine or isopropyl alcohol hypersensibility patients * If any patients changed its mind after signing the informed consent will be removed from the study.

Design outcomes

Primary

MeasureTime frameDescription
Surgeon's global satisfaction with the applicators.IntraoperativeUsing an analog visual scale we will record the total score, over a maximum of 80 points, that assess the following quality aspects of the applicators: * Satisfaction with the presentation of the product * Satisfaction with the simplicity of activation * Satisfaction with the mix of the different components of the product * Satisfaction with the comfort of product use * Satisfaction with the surface covered by an applicator * Satisfaction with the shape of the applicator for painting areas of difficult access * Satisfaction with the drying time of the product * Satisfaction with the area delimited with the use of the product
Qualities of each applicatorsIntraoperativeUsing an analog visual scale, were one end represents totally disagree and the other totally agree (0-10 points), we will record the score of each of the following quality aspects of the applicators: * Satisfaction with the presentation of the product * Satisfaction with the simplicity of activation * Satisfaction with the mix of the different components of the product * Satisfaction with the comfort of product use * Satisfaction with the surface covered by an applicator * Satisfaction with the shape of the applicator for painting areas of difficult access * Satisfaction with the drying time of the product * Satisfaction with the area delimited with the use of the product

Secondary

MeasureTime frameDescription
Costs of using the applicatorsThrough study completion, an average of 3 months
Adhesion to preoperative measures to avoid surgical site infections (SSI)Through study completion, an average of 3 monthsAnalyze the verification check list for surgical site infection preoperative prevention. This check list has been provided by the Preventive Medicine, Public Health and Hygiene Spanish Society as part of the Zero Surgical Site Infection Protocol. This verification check list includes indicators of: * Antibiotic prophylaxis * Intraoperative Alcoholic Chlorhexidine application * Hair removal from the surgical site * Normotherapy * Glycemic control
Surgical site infection incidenceDuring the first 30 to 90 days after surgery, according to the SSI prevention protocol

Contacts

Primary ContactCristina Fernandez Perez, Ph D.
cfernandezp@salud.madrid.org+34913303430

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026