Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04250649
Other study ID # 2020-00170
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 31, 2020
Est. completion date March 31, 2024

Study information

Verified date January 2020
Source Hôpital du Valais
Contact Nicolas Gallusser
Phone 027 603 90 00
Email gallussern@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Propionibacterium acnes is a pathogen commonly identified in postoperative shoulder infections. A recent study has shown that P. acnes is likely to be disseminated in the operating field from the subcutaneous layer by the manipulation of soft tissues by the surgeon and the instruments. Disinfection of the subcutaneous tissue seems to significantly reduce contamination of the operating field during primary shoulder surgery. This study seeks to assess the efficacy of disinfection of the subcutaneous tissue compared to dissection with an electrosurgical unit on P. acnes contamination during primary shoulder surgery.


Description:

The investigators are going to study the efficacy of disinfecting the subcutaneous tissue with Betadine standard solution during primary shoulder surgery compared to electrosurgical dissection. They will randomize 105 patients on two arms. The control group receiving no disinfection of the subcutaneous tissue but a dissection with an electric cautery(A) and intervention group receiving a disinfection of the subcutaneous tissue (B). They believe that the duration of 4 years is sufficient to recruit the number of patients necessary for this study.

All patients 18 years of age or older admitted to Valais Hospital for primary shoulder surgery and having signed the consent of the study will be eligible.

The use of disinfection of the subcutaneous tissue during primary shoulder surgery could reduce contamination of the operating field and theoretically the post-operative infection rate after primary shoulder surgery.

The study focuses on disinfection with Betadine solution of the subcutaneous tissue during primary shoulder surgery. This action could decrease contamination of the operating field and the infection rate after primary shoulder surgery.

This solution is already widely used for disinfecting the skin and traumatic or surgical wounds.

The investigators will use it according to the recommendations made in the Swiss Compendium of Medicines.

No evidence has been brought to a decrease in this contamination if the dissection is carried out with an electric cautery. Scalpel dissection is used as standard in orthopedic surgery as well as in other surgical disciplines.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 105
Est. completion date March 31, 2024
Est. primary completion date March 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. = or> 18 years old

2. treated at the Valais Hospital for primary shoulder surgery.

3. have signed the consent

Exclusion Criteria:

1. <18 years old

2. History of shoulder surgery

3. History of shoulder infection

4. Antibiotic therapy in the 2 weeks preceding the intervention

5. Cortisone infiltration in the 6 months preceding the intervention

6. Allergy to iodinated contrast agent or Cefuroxime

7. Allergy to povidone iodine complex or other contraadication to Betadine

8. Refusal of study terms

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
subcutaneous tissue disinfection
Skin and subcutaneous incision (up to the muscular fascia) with "superficial blade" scalpel, disinfection of the subcutaneous tissue with 3cc of Betadine solution, placement of the retractors, dissection and development of the delto-pectoral interval with "deep blade" scalpel. When the joint is opened, bacteriological smears are taken from 5 sites in the two groups. 1) exposed subcutaneous tissue, 2) surgeon's gloves (distal end of fingers), 3) "superficial blade", 4) "deep blade", 5) retractors. The rest of the shoulder surgery procedure does not differ from what is commonly performed. The samples are sent to bacteriology for bacterial culture. Anaerobic research is done specifically for P. acnes. The results are considered negative after 10 days.

Locations

Country Name City State
Switzerland Hôpital du Valais Martigny Valais

Sponsors (1)

Lead Sponsor Collaborator
Hôpital du Valais

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary positive sample Compare the positive bacteriological sample rate during an open shoulder surgery procedure with a disinfection of the subcutaneous tissue compared to an operating procedure without disinfection but dissection with an electric knife. 4 years
See also
  Status Clinical Trial Phase
Recruiting NCT06202053 - An Observational Study on the Quality of Life After Precise Lung Resection Through the Periareolar Incision
Terminated NCT05234632 - Study to Evaluate the PICO 14 Negative Pressure Wound Therapy System in the Management of Acute and Chronic Wounds N/A
Completed NCT04888624 - A Comparison Between Two Post-operative Dressings N/A
Recruiting NCT05897723 - Fractional Radiofrequency for Reduction of Surgical Scar Formation N/A
Recruiting NCT03561376 - Zinc Oxide Versus Petrolatum Following Skin Surgery Early Phase 1
Active, not recruiting NCT05028816 - Force Modulating Tissue Bridges for Closure of Vertical Scars in Breast Reduction N/A
Terminated NCT03688880 - A Clinical Study to Compare MAR-CUTIS With Dermabond Advanced N/A
Recruiting NCT02989363 - Evaluation of the Use of Resources and Costs N/A
Completed NCT03199911 - Topical Antibiotic Prophylaxis for Eyelids Phase 4
Recruiting NCT05618912 - Scar Appearance After Postoperative Hydrocolloid Dressing Versus Standard Petrolatum Ointment N/A
Withdrawn NCT04053946 - Clinical Assessment of Next Science Wound Gels in Healing Below the Knee Amputation Surgical Wound Compared to SOC N/A
Enrolling by invitation NCT05461157 - Preoperative Silicone Ointment and Wound Healing N/A
Completed NCT04336371 - Exploratory Prospective of Experienced by Patients in the Surgery of Skin Cancers of the Face in Interventional Dermatology Department
Completed NCT03860181 - Dermabond PRINEO for Total Shoulder Arthroplasty N/A
Enrolling by invitation NCT03180346 - A Prospective, Randomized, Comparative Study to Assess the Prevention of Surgical Site Infection (SSI's) in Revision Total Joint Arthroplasty Patients Treated With Single-Use Negative Pressure Wound Therapy (PICO) or Standard Care Dressings (AQUACEL Ag SURGICAL Dressing). N/A
Not yet recruiting NCT05687942 - The REBUILD Trial: Closure of the Abdominal Wall N/A
Completed NCT02977221 - Efficacy of Piezosurgey Corticotomy (a Minimally Invasive Surgical Technique) in Accelerating Orthodontic Alignment N/A
Completed NCT02975765 - Evaluation of the Levels of Pain and Discomfort Between Two Methods of Correcting Misaligned Teeth N/A
Completed NCT06047418 - Blepharoptosis in Indonesia: A 5-Year Multicenter Study on Characteristics and Surgical Evaluation
Not yet recruiting NCT04894604 - A Safety and Performance PMCF Investigation of the Avance® Solo NPWT System in Surgically Closed Incisions N/A