Biofilm

2

Review clinical trials related to Biofilm. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effects of Biocidin on Oral Biofilms

The primary purpose of this study is to evaluate the effects of Biocidin liquid on oral biofilms among healthy adults. A single-arm, open-label prospective study will be conducted evaluating the impact of two weeks of supplementation with label dosing of Biocidin liquid on oral biofilms as assessed by SimplyPERIO (Spectrum Solutions, Salt Lake City, UT).

Participants needed: 60
Trial details
Age: 25+Biological sex: AllType: InterventionalSponsor: OvationLabUpdated: Mar 11, 2026Locations: 1
Eligibility criteria

Adult females or males age ≥ 25 years [+5]

Current use of oral Biocidin or botanical mouthwash [+5]

Status: Not yet recruiting

Efficacy of a Polyhexanide Biguanide-Based Gel in the Prevention of Biofilm Formation in Pressure Ulcers

INTRODUCTION: Pressure ulcers (PU) are one of the main challenges for nursing in our country. Wound bed preparation and the TIME algorithm provide essential tools for adequately treating these lesions. However, these wounds tend to become chronic due to the bacterial load in their bed. It is now known that bacteria can form complex and diverse structures, named as biofilm, which are difficult to diagnose and much more resistant to antimicrobial action. Controlling these biofilms is crucial to create the optimal conditions for wound healing. Currently, it is believed that biofilms are present in 60-100% of chronic wounds. Therefore, more studies are needed to evaluate the efficacy of different antimicrobial agents on these structures. OBJECTIVE: To determine the efficacy of a gel containing polyhexanide and biguanide, alone or in combination with alginate with or without silver, in preventing biofilm in PU, in terms of healing at 4 weeks. METHODOLOGY: Multicenter clinical trial with a 2x2 factorial design, conducted with patients from Alcoy with category II and III PUs that meet the inclusion and exclusion criteria. A sample of 140 participants is estimated, distributed into four groups of 35 patients. The interventions that will be carried out will be: application of Prontosan gel® and Aquacel Ag+®; Aquacel Ag+®; control group; Prontosan gel®. Data on wound evolution will be collected using RESVECH 2.0. Descriptive statistical analysis and hypothesis testing will be performed.

Participants needed: 140
Trial details
Phase: Early Phase 1Age: 65+Biological sex: AllType: InterventionalSponsor: Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat ValencianaUpdated: Feb 10, 2026
Eligibility criteria

Bedridden patients, patients with bed-to-chair mobility, or those in a wheelchai... [+5]

Patients who, despite the above, present a deteriorated health status that could... [+2]