Skip to main content
MedPathMedPath Home
Clinical Trials/DRKS00023178
DRKS00023178
Completed
未知

Prospective diagnostic study comparing the rotation / torsion determination on the lower extremity using CT and MRI - RoCT-MR study

niversitätsklinikum Tübingen0 sites26 target enrollmentNovember 17, 2020
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
ConditionsM22.0M22.1M22.2M84.05M84.06M21.85M21.86M21.89M21.95M21.96M21.75M21.76Recurrent subluxation of patellaRecurrent dislocation of patellaPatellofemoral disorders

Overview

Phase
未知
Intervention
Not specified
Conditions
M22.0
Sponsor
niversitätsklinikum Tübingen
Enrollment
26
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 17, 2020
End Date
August 9, 2022
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversitätsklinikum Tübingen

Eligibility Criteria

Inclusion Criteria

  • •Suspected rotational / torsional misalignment of the lower extremity and clinical indication for rotation / torsion determination using CT
  • •After the justifying indication has been established by radiology, a CT rotation / torsion determination of the entire lower extremity has been successfully carried out
  • •No metallic or ferromagnetic implants in the entire lower extremity
  • •Age of the patient at the time of study inclusion \= 18 years.
  • •Patient consent

Exclusion Criteria

  • •Non\-existent or revoked consent of the patient
  • •Pregnant / breastfeeding women
  • •Presence of non\-MRI\-compatible implants or any kind of metal in and on the body (e.g. pacemakers, artificial heart valves, metal prostheses, implanted, magnetic metal parts, coils, etc.)
  • •People who report a hearing impairment or an increased sensitivity to loud noises
  • •People with reduced temperature sensation and / or increased sensitivity to warming of the body
  • •People suffering from claustrophobia
  • •People who do not want to be informed about incidental findings

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
An observational study for comparison of diagnostic yield, maneuverability and safety between 22-gauge and 25-gauge needles for endobronchial ultrasound-guided transbronchial needle aspiration.malignant and benign mediastinal hilar lymphadenopathy.
JPRN-UMIN000034705Matsusaka Municipal Hospital60
Not yet recruiting
Not Applicable
Comparison of survival between acetate-containing bicarbonate dialysate and acetate-free bicarbonate dialysate containing citrate in hemodialysis with type II dialyzer and online hemodialysis
JPRN-UMIN000053090Others700
Not yet recruiting
Not Applicable
Study for comparison between membrane materials on survival in super high flux hemodialysis and online hemodiafiltratio
JPRN-UMIN000051791Social medical corporation, Kawashimakai, Kawashima hospital700
Not yet recruiting
Not Applicable
An Observational study to compare the clinical outcomes of Ventilator Associated Events among COVID-19 and non COVID ICU patients.Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere
CTRI/2021/08/035444ilavati hospital and research centre
Not yet recruiting
Not Applicable
A study to compare the patient reported outcomes with the use of oral dydrogesterone vs. micronized vaginal progesterone in high risk pregnanciesHealth Condition 1: O092- Supervision of pregnancy with other poor reproductive or obstetric history
CTRI/2022/11/047511Emcure Pharmaceuticals Ltd