Is NCT07116174 recruiting in Fresno, CA?

Yes, NCT07116174 is currently recruiting participants at its Fresno, CA location. This diabetic foot ulcer (dfu) clinical trial is actively enrolling qualified participants.

How do I join the diabetic foot ulcer (dfu) clinical trial in Fresno?

To join this clinical trial in Fresno, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Fresno clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Diabetic Foot Ulcer (DFU) Clinical Trial in Fresno, CA

About This Diabetic Foot Ulcer (DFU) Study in Fresno

The goal of this clinical trial is to evaluate the clinical outcomes of Diabetic Foot Ulcers (DFUs) treated with a weekly application of Xcell Amnio MatrixTM (XAM) as adjunct to standard of care (SOC) compared to SOC alone in male and female over the age of 18 years old. The main question it aims to answer is: What is the proportion of subjects with complete wound closure during the 12 weeks of the treatment phase? Participants: * Will be screened and re-screened after 2 weeks to be assessed whether they meet the eligibility criteria * Eligible subjects will receive study product application, and for 12 weeks will return to the clinic once every 7 days (±3 days) for treatment visits * Subjects who complete the treatment will be followed up after 2 weeks

Sponsor: New Horizon Medical Solutions

Who Can Participate

Inclusion Criteria

Subjects will be eligible for enrollment in the study only if they meet ALL the following criteria at time of Screening:

Subject is 18 years of age or older.

Subject has diabetes mellitus (Type 1 or Type 2), requiring insulin or oral/injectable medications to control blood glucose levels

Glycosylated hemoglobin (HbA1c) level is \<12% Note: Prior documented HbA1c within 12 weeks of Screening is acceptable.

Duration of ulcer is ≥ 4 weeks but ≤ 1 year, unresponsive to SOC

Ulcer area is ≥ 1.5cm2 and ≤ 20cm2 and with a clean, granulating base with minimal adherent slough at the Baseline Visit

Ulcer location is at or below the ankle (malleolus)

Subject is amenable to use of off-loading, as needed for plantar ulcer

Ulcer extends through the full thickness of the skin but not down to muscle, tendon, or bone

Subject is at least 12 weeks post lower extremity revascularization procedure, if one has been performed.

Subject is in general good health, with no clinically significant medical conditions or abnormalities that, in the opinion of the Investigator, would interfere with study participation, the assessment of study endpoints, or pose additional risk to the subject.

Adequate circulation to the affected lower extremities as demonstrated by one of the following within 12 weeks of screening:

Dorsum transcutaneous oxygen measurement (TCOM) ≥ 30 mmHg,

Skin perfusion pressure (SPP) measurement ≥ 30 mmHg,

Ankle-Brachial Index (ABI) ≥0.7 and ≤1.2, OR

Toe-Brachial Index (TBI) ≥ 0.6

Subject is willing to use an acceptable method of contraception throughout the duration of the trial, if of childbearing potential. Acceptable methods of contraception include abstinence, female subject/partner's use of hormonal contraceptive (oral, patch, injectable, depot or vaginal) in conjunction with a barrier method (e.g., diaphragm, cervical cap, condom, spermicide or sponge), or female subject/partner's use of an implantable device (implantable rod or intrauterine device). Female subject/partners of non-childbearing potential are defined as surgically sterile (e.g., bilateral tubal ligation, hysterectomy) or two years postmenopausal at time of screening. All male subjects (excluding men who have been sterilized) with female partners of child-bearing potential must agree to consistently and correctly use a condom for the duration of the study. In addition, subjects may not donate sperm for the same time period.

Subject is able to read, understand and sign the informed consent form (ICF).

Subject is available and willing to complete all study assessments and can comply with standard of care (debridement, dressing changes etc.) as applicable.

Exclusion Criteria

Subjects meeting ANY of the following criteria at time of Screening will be excluded from enrollment:

Clinical evidence of ongoing infection and/or receipt of IV, oral, or topical antimicrobials.

Wheelchair bound or bed-ridden (ambulatory with assistance is acceptable).

Ulceration at the site of amputation.

Undergoing renal dialysis.

Known or suspected malignancy in the target ulcer, or a history of cancer in the preceding 5 years (other than carcinoma in situ of the cervix or adequately treated non-melanoma skin cancer).

Documented history of osteomyelitis at the target ulcer location within 6 months of screening.

History of radiation at the ulcer site.

New York Heart Association Class III or IV congestive heart failure or uncontrolled cardiac dysrhythmia.

Diagnosis of autoimmune disease(s) (rheumatoid arthritis, lupus, psoriasis, Sjogren's syndrome) or arthritis requiring corticosteroid treatment.

Subject has received in the past 4 weeks or is scheduled to receive any of following medication or therapies during the course of the study:

Immunosuppressants (including chronic systemic corticosteroids or application of topical steroids to the ulcer surface)

Cytotoxic chemotherapy

Growth hormone

Oral or systemic antifungal or antituberculosis treatment

Use of any investigational drug(s) or therapeutic device(s)

Target ulcer(s) previously treated with negative pressure, hyperbaric oxygen, or tissue engineered materials (e.g., Apligraf®, EpiFix® or Dermagraft®) or other scaffold materials (e.g., Oasis, Matristem) within 4 weeks prior to screening.

Target ulcer(s) anticipated to require negative pressure wound therapy or hyperbaric oxygen at any time during the study.

Healing of target ulcer is observed to be ≥35% at the end of the Run-in Period (between Screening and Baseline Visits)

Subject is pregnant or breastfeeding.

Presence of any other condition(s) which seriously compromises the subject's ability to complete this study or has a known history of poor adherence with medical treatment.

Active Charcot foot (stable chronic Charcot foot is not exclusionary).

Ulcers on toes 2, 3, 4, and/or 5 only (ulcer on plantar surface of the great toe only is not exclusionary).

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Fresno?

Yes, this clinical trial (NCT07116174) has an active research site in Fresno, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Diabetic Foot Ulcer (DFU) Treatment Options in Fresno, CA

If you're searching for diabetic foot ulcer (dfu) treatment options in Fresno, CA, this clinical trial (NCT07116174) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Fresno research site is actively enrolling participants for this clinical trial. You'll receive care from experienced diabetic foot ulcer (dfu) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all diabetic foot ulcer (dfu) clinical trials near you to find additional studies recruiting in your area.

Diabetic Foot Ulcer (DFU) Clinical Trial in Fresno, CA

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