Cysto-position: Does Position Influence the Diagnosis of Detrusor Overactivity in a Neurological Population

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05949567
Collaborator
(none)
160
1
2
24
6.7

Study Details

Study Description

Brief Summary

ICS (International Continence Society) recommendations published in 2017 recommend performing urodynamic examinations in the sitting or standing position. These recommendations are based on a review of the literature published in 2008, which has several limitations: heterogeneous populations, old and non-harmonized techniques, and very few neurological patients. It seems appropriate to focus on neurological patients and to examine the influence of position on the detection of detrusor overactivity in these patients.

The point here is to reexamine the ICS recommendations, which are not designed for neurological patients. Indeed, many patients suffering from Multiple Sclerosis (MS) or Parkinson's disease are unable to sit or stand for the duration of the urodynamic examination. The investigators would like to assess whether exploring sphincter disorders in the supine position is still interpretable.

This would enable us to define ICS good practice recommendations for a neurological population.

Condition or Disease Intervention/Treatment Phase
  • Other: urodynamic exam in sitting and lying position
N/A

Detailed Description

1st consultation (selection - D-15):

  • Targeted questioning of disorders, completion of USP self-questionnaire, and UPDRS or EDSS scales as part of care.

  • Verification of ultrasound results (for men).

  • Schedule Urodynamic Assessment as part of treatment.

  • Verification of eligibility criteria

  • Partial information of the patient (or relative/guardian/guardian if applicable) to limit bias, and a period of reflection prior to the urodynamic test to collect consent.

On the day of the Urodynamic Assessment (D0):
  • Written, free and informed consent.

  • Data collection by a physician trained in the study,

  • Randomization of patient to determine starting position (lying or sitting) for urodynamic assessment (via CleanWeb).

  • Urodynamic assessment according to ICS recommendations, with constant filling speed over the 2 fillings (50 ml/min), water filling - Laborie machine - T-Doc system in both positions in the order defined by randomization, and printout of curves.

  • Entry of socio-demographic data.

  • Curves reread by a doctor who had not performed the examination and who did not know the patient or the starting position (single blind).

  • Completion of the paper file by the physician reading the curves, with the following data for position 1 and position 2:

  • Volume at B1 and B3 (in ml)

  • Basal bladder pressure (cm / H2O)

  • Occurrence of CNID or mictional reflex arc (diagnosis of detrusor overactivity)

  • Volume of leakage or 1st NIDC (Uninhibited Detrusor Contraction) (ml) or

  • Bladder pressure at leakage (cm / H2O)

  • Maximum bladder pressure (cm / H2O)

  • Paper data entry on Excel database by a trained investigator declared on the study

Study Design

Study Type:
Interventional
Anticipated Enrollment :
160 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Diagnostic
Official Title:
Does Position Influence the Diagnosis of Detrusor Overactivity in a Neurological Population - a Concordance Study Between Lying and Sitting Position
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2025
Anticipated Study Completion Date :
Oct 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Lying position first - then sitting position

Other: urodynamic exam in sitting and lying position
Urodynamic exam with 1st filling in sitting or lying position. Then , during the same procedure, a second filling in the opposite position of the 1st filling (lying or sitting)

Experimental: Sitting position first - then lying position

Other: urodynamic exam in sitting and lying position
Urodynamic exam with 1st filling in sitting or lying position. Then , during the same procedure, a second filling in the opposite position of the 1st filling (lying or sitting)

Outcome Measures

Primary Outcome Measures

  1. concordance diagnosis of detrusor overactivity between lying and sitting position [24 months]

    Measurement concordance of detrusor pressures using the intraclass correlation coefficient statistic

Secondary Outcome Measures

  1. position influence on the overactive detrusor gravity between the 2 positions [24 months]

    Measurement of the concordance of detrusor overactivity diagnostic gravities during urodynamic assessments, between those performed in the supine position and those performed in the seated position. Concordance will be assessed using Cohen's Kappa statistic.

  2. Evaluation of the diagnosis quality of the detrusor overactivity between the 2 position [24 months]

    Measurement of the diagnostic quality of urodynamic testing performed in the supine position in neurological patients to detect detrusor activity, with the seated position being the gold standard: estimation of sensitivity and specificity.

  3. comparison of the distribution of detrusor overactivity diagnoses according to position. [24 months]

    Measurement of the association between position during urodynamic assessment and diagnosis of detrusor overactivity: comparison of the distribution of diagnoses of detrusor overactivity according to position.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient with MS or neurologically confirmed Parkinson's disease, with indication for urodynamic assessment - 1st assessment

  • Clinical overactive bladder syndrome with USP overactive bladder sub-score > or = 4 - Age ≥18 years

  • In men: no prostatic hypertrophy on ultrasonography

  • In women: no stress urinary incontinence (SUI); USP SUI subscore ≤ 2

  • Affiliated with a social security scheme (excluding AME).

  • Free and informed written consent

Exclusion Criteria:
  • Opposition to the performance of a Urodynamic exam as part of treatment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Physical and Rehabilitation Medicine Pitié Salpêtrière Hospital Paris France 75013

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT05949567
Other Study ID Numbers:
  • APHP230769
First Posted:
Jul 18, 2023
Last Update Posted:
Jul 25, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 25, 2023