Site Infection

3

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

Condition / disease
Location
Status: Not yet recruiting

Incidence of Ssi After c.s

aim of the work is to evaluate adherence to preoperative , intraoperative, and postoperative infection preventive measures during cesarean section and to assess it s impact on the incidence of surgical site infection and maternal well-being during 30 days postoperative peroid.

Participants needed: 105
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Assiut UniversityUpdated: Mar 17, 2026Locations: 1
Eligibility criteria

All women who underwent cesarean section during the study period

Patients who are lost to follow-up before completion of the 30-day postoperative...

Status: Not yet recruiting

Vaginal Microbiota and Post-cesarean SSI

The goal of this observational study is to investigate the relationship between vaginal microbiota composition and the development of post-cesarean section wound infection in women undergoing cesarean delivery. The main question it aims to answer is: Is there a correlation between specific vaginal microbiota profiles and the incidence of post-cesarean section wound infection? Can specific bacterial taxa or diversity indices within the vaginal microbiota predict the risk of post-cesarean section wound infection? Participants will: Provide vaginal swab samples pre-operatively and post-operatively. Undergo standard post-cesarean section care and follow-up. Have wound assessment performed per standard of care, and have data collected regarding wound infection status. Have demographic and clinical data collected, including but not limited to, antibiotic use, gestational age, and comorbidities.

Participants needed: 160
Trial details
Age: 18-40Biological sex: FemaleType: ObservationalSponsor: Al-Azhar UniversityUpdated: Jun 15, 2025Locations: 1
Eligibility criteria

Pregnant women undergoing elective or emergency cesarean section (CS). [+2]

Use of antibiotics within two weeks prior to delivery. [+3]

Status: Recruiting

Irrisept Solution for Instrumented Spine Surgery

Various spine surgeons perform wound irrigation using saline mixed with vancomycin, relying on mechanical debridement of non-viable tissue, physical disruption of biofilm, and bacteriostatic effect against gram positive flora. When used as a powder, topical application of vancomycin has demonstrated increased risk of symptomatic seroma formation, which is an adverse outcome that often requires bedside or intra-operative aspiration. Broad-spectrum antiseptic agents, such as Irrisept, offer bacteriocidal properties to eliminate hardware inoculation, thereby minimizing the risk of deep space infection, while obviating the risk of seroma development.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Rhode Island HospitalUpdated: Nov 20, 2024Locations: 1
Eligibility criteria

Age: 18+ years old [+3]

Acute/chronic open wounds (spine or non-spine) [+7]