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RecruitingNCT07554313TORSADOUpdated May 20, 2026

Analysis of Factors Associated With Delayed Medical Consultation for Testicular Torsion Among Adolescents in the Haut-Rhin Department Between 2020 and 2025

An observational study in Testicular Torsion and Adolescent, sponsored by Centre Hospitalier de Colmar. Recruiting at 1 site in France. Open to male participants aged 10 Years to 17 Years. Per ClinicalTrials.gov, last updated 2026-05-20.

Sponsored by Centre Hospitalier de Colmar · Observational

From the registry’s dates

  • Started May 2026; still recruiting 5 months later.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
150
Ages
10 Years to 17 Years
Sex
Male
01

Study summary

The objective of this observational study is to identify the factors that influence whether or not an adolescent seeks immediate medical attention upon the onset of symptoms of testicular torsion. The main question it aims to answer is as follows:

What factors are associated with a delay in seeking medical care-defined as a time interval of 6 hours or more between the onset of symptoms and the first visit to Colmar Hospital-among adolescents aged 10 to 18 who underwent surgery for testicular torsion?

Participation in this study involves completing a questionnaire: the "Questionnaire for Assessing Factors Associated with Delay in Seeking Medical Care for Testicular Torsion in Adolescents."

02

Conditions studied

  • Testicular Torsion
  • Adolescent
03

In context

Lead sponsor

Centre Hospitalier de Colmar is the lead sponsor of 5 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 17 Years
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Teenagers attending at Colmar Hospital

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients who underwent surgery for suspected testicular torsion between 2020 and 2025 in the Paediatric Surgery Department of the Hôpitaux Civils de Colmar, following admission via the Paediatric A\&E Department of the same hospital;
  • Patients aged between 10 and 17 years at the time of admission;
  • Participants who, after being informed, do not object to the use of their data for the purposes of this research;
  • Holders of parental authority who, after being informed, do not object to the use of their children's data for the purposes of this research.

Exclusion criteria

Exclusion Criteria:

  • Any intraoperative diagnosis other than testicular torsion (e.g. hydatid torsion);
  • Patients who cannot read and/or understand French;
  • Participants or legal guardians who have expressed their refusal to take part in the study;
  • Unusable patient records: insufficient data.
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
150 participants (estimated)
Patient registry
No

Groups and cohorts

  • Early consultation

    Patients who attended within strictly less than 6 hours of the onset of symptoms

    Other: Questionnaire

  • Delayed consultation

    Patients who attended within six hours or more than the onset of symptoms.

    Other: Questionnaire

Interventions

  • OtherQuestionnaire

    Questionnaire for Assessing Factors Associated with Delay in Seeking Medical Care for Testicular Torsion in Adolescents

06

What researchers measure

Primary outcomes

  1. The presence of at least one reported barrier to accessing healthcare

    The primary outcome measure is the presence of at least one reported barrier to seeking healthcare, encompassing the reasons for delay cited by patients (embarrassment or shame about discussing symptoms, fear of hospitals, fear of being a bother, downplaying symptoms, or other reasons).

    Time frame: Before the first attending for testicular torsion

Secondary outcomes

  1. The association between patients' prior knowledge of testicular torsion and the time taken to seek medical advice

    The patient's prior awareness of the need to seek urgent medical attention in the event of acute testicular pain, assessed by a binary response (yes/no) to the questionnaire.

    Time frame: Before the first attending for testicular torsion

  2. The influence of the initial perception of symptom severity on the time taken to seek medical advice.

    The initial subjective perception of symptom severity, assessed using an ordinal scale in response to the question 'When these symptoms/signs first appeared, how did you perceive them?' and analysed categorically. The scale is ranges from 0 = 'Not serious', 1 = 'Slightly serious, 2 = 'Moderately serious' to 3 = 'Extremly serious'. A higher score reflects higher perception of severity.

    Time frame: Before the first attending for testicular torsion

  3. The role of those close to the individual, particularly parents or legal guardians, in the decision to seek medical advice.

    Immediate notification by an adult (parent or legal guardian) as soon as symptoms appear, measured as a binary variable (yes/no).

    Time frame: Before the first attending for testicular torsion

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started May 2026 (actual). Primary completion is estimated for Sep 2026, 4 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 21, 2026
First posted
Apr 28, 2026
StartActual
May 13, 2026
Primary completionEst.
Sep 30, 2026
CompletionEst.
Dec 31, 2026
Last update
May 20, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07554313
Lead sponsor
Centre Hospitalier de Colmar
Responsible party
Sponsor
First posted
Apr 28, 2026
Start date
May 13, 2026
Primary completion
Sep 30, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
May 20, 2026

Study contacts

Nicolas Sachnine
Contact
nicolassachnine@gmail.com
+33389126080
Magali Eyriey
Contact
cellule-promotion@ch-colmar.fr
+33389124810
Dorine Combescot
study director · Hopitaux Civils de Colmar
Sandy Jochault-Ritz
principal investigator · Hopitaux Civils de Colmar

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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