The Surgical Research Organisation
ProSurg is an international Clinical Research Organisation (CRO) offering a complete set of clinical research services, to help you navigate the complexities of clinical research with confidence and to provide solutions tailored to your needs, whether you are a big or small medical device company, a medical professional, or a scientific society.
Surgical Site Visits
Study Monitoring
Ethical & Regulatory Approvals
Statistical Analysis
Scientific & Medical Writing
Project Management
Why do you need a CRO?
To perform retrospective studies
To perform prospective studies
To perform ambispective studies
To perform clinical investigations for pre or post-market approval
To assist with regulatory affairs, clinical trial planning, site selection and initiation, recruitment support, clinical monitoring, data management, trial logistics, biostatistics, medical writing, and project management.
Recently published clinical trials
Effect of preoperative coronary CT for planning of percutaneous coronary intervention for complex chronic total occlusion (CTS-C-CTOPCI): study protocol for an open-label randomised controlled trial
La Scala et al., Trials, August 2023
The purpose of this randomised controlled trial is to determine whether improved planning of CTO‐PCI using coronary computed tomographic angiography (CCTA) (versus conventional angiography) increases success rates of wire crossing in ≤ 60 min in difficult cases.
Limited fasciectomy with versus without autologous adipose tissue grafting for treatment of Dupuytren’s contracture (REMEDY): study protocol for a multicentre randomised controlled trial
Sawaya et al., Trials, 2024
The purpose of this multicentre randomised controlled trial is to evaluate outcomes of limited fasciectomy with autologous adipose tissue grafting (experimental group) versus limited fasciectomy alone (control group) for treatment of Dupuytren’s contracture.