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Acute scrotal pain due to testicular torsion is a rare but urgent urological condition that requires immediate surgery to prevent permanent damage or loss of the testicle. Early detection is crucial to minimize delays from the onset of pain to operative treatment. The diagnosis of torsion involves a combination of physical examination and imaging studies, such as Doppler ultrasound (DU). However, DU requires an experienced radiologist and may cause unnecessary time delays. Thermal imaging is a noninvasive technique that can detect skin surface temperature variations using a highly sensitive infrared camera. Although there are some promising animal studies using thermal imaging for the diagnosis of testicular ischemia, number of studies in humans is very limited.
According to a small pilot study in 2024, thermal imaging is a fast, feasible and noninvasive diagnostic tool that seems to have considerable potential in the evaluation of patients with acute testicular pain, especially those with symptoms of testicular torsion. However, further research with a larger sample size is needed. In this multicenter study, the investigators aim is to determine the role of thermal imaging in the diagnosis of acute testicular pain.
Males with acute testicular pain entering emergency are included. After informed consent thermal image of testicles will be taken before any additional investigations such as laboratory tests and DU. Participants are treated as usual and testicular temperatures will be correlated with final diagnosis after approximately 6-month study period is over.
Full description
Acute testicular pain can have several causes, such as testicular torsion, but current diagnostic methods, such as DU, may be time-consuming and operator-dependent. The aim of this study is to evaluate the use of thermal imaging as a diagnostic tool for acute testicular pain, particularly in diagnosing testicular torsion, which requires urgent surgical treatment. Thermal imaging is a quick and non-invasive alternative that may help to reduce diagnostic delays. Results from two animal studies and a small pilot study conducted on patients in 2024 suggest that a thermal camera may be able to distinguish testicular torsion from epididymitis, which is another common cause for acute testicular pain. This multicenter study investigates the usability, accuracy, operator independence, and clinical applicability of thermal imaging in diagnosing acute testicular pain. According to a preliminary calculation, at least 146 participants are required with 80% statistical power and a 5% error rate. The sample size will be reassessed after six months, and if necessary, the enrollment phase will be extended.
A prospective 6-month study on the use and feasibility of thermal imaging for the diagnosing the cause of acute testicular pain will be conducted. Participating centers will include all university hospitals in Finland (Helsinki, Turku, Oulu, Tampere and Kuopio) and central hospitals of Seinäjoki, Jyväskylä and Pori. The study population will include all male participants presenting with acute testicular pain.
Participants with testicular pain are examined with thermal imaging immediately after arriving in the emergency department and before any other examinations (e.g., laboratory tests, DU). The results of the thermal imaging are not used in clinical decision-making; instead, they are compared later with the final diagnosis. Thermal imaging therefore does not influence the examinations or treatment decisions made for the participants, nor does it expose the participants to harmful ionizing radiation.
After entering the emergency room, the participants are verbally informed of the ongoing study and given research information sheet and preparatory instructions concerning the potential thermal imaging. The instructions explain how to tape the penis upward against the abdomen for 5 minutes to eliminate its thermal effect on the thermal image of the testicles. The trained and delegated research staff members give further verbal information about the study and the thermal imaging. Afterwards they collect the verbal permission and a signed informed consent form to take the thermal image. Participant's social security number, date, time and the code of the thermal image are written down on the consent form, which is stored in a secure place for safekeeping. Duplicate of the consent form remains with the participants. The estimated time needed for taking the thermal image is few minutes. Temperature results, however, will have no effect on decision making, as participants will be diagnosed and treated as usual using established routine diagnostic tools such as clinical evaluation, laboratory and urinary testing and DU.
A class IIa CE-approved Thermidas handheld camera (IRT-384 Tablet) will be used. It is designed for healthcare professionals to monitor and evaluate skin surface temperatures. The company Thermidas will educate our research staff in the use of their thermal camera. The leasing cost is 500 € per camera per month and it is covered by reaserch funf of Tampere University Hospital. The role of the company Thermidas in this study is to solely provide the thermal cameras for a fee, including the education in the use of the camera, and to store the images securely. The investigators have got a authorization for medicinal device from Fimea and approval from the ethics committee of Tampere University Hospital.
Technical specifications of the IRT-384 camera:
The distance from the camera to the scrotum is approximately 20 cm while participant is standing, and testicles are hanging freely. Results of thermal imaging (temperature difference between testicles in Celsius) will be correlated with final diagnose at the end of study. Thermal picture (testicular temperatures) will be analyzed by two independent investigators blinded to each other and results will be correlated with the final diagnoses. SPSS statistical software will be used and sensitivity and specificity for thermal imaging will be calculated. Study registry holder will be Central Hospital of Seinäjoki.
Sub-study 1 Adult participants having funicular orchiectomy due to testicular cancer will be included. At operation thermal picture of untouched testicles will be taken before ligation or closure of the funicle (baseline) and at 5, 10 and 15 minutes afterwards. After this, funicular orchiectomy is performed as usual.
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Inclusion criteria
Sub-study 1: Adult males, who are having funicular orchiectomy due to testicular cancer and sign informed consent.
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150 participants in 1 patient group
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Central trial contact
Mika P Raitanen, M.D, Ph.D, associate professor
Data sourced from clinicaltrials.gov
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