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Clinical Trials/CTRI/2024/02/063285
CTRI/2024/02/063285Not yet recruitingNot Applicable

Decoding urinary incontinence with an algorithm

Not provided1 site in 1 country320 target enrollmentStarted: March 15, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
320
Locations
1
Primary Endpoint
its a simple and doable algorithm

Study Overview

Brief Summary

To Women presenting in the OPD with urinary incontinence for the very first time  detailed description of study procedure will be given and willing participants will be recruited after Informed written consent .Simple history and symptom based questions will be asked in a stepwise manner,which has focussed questions like whether its continuous,intermittent,or any preceding event/insult,whether is able to evacuate completely from time to time.Symptoms of exclusion will also be asked to rule out specific type of incontinence. After arriving at a diagnosis ,recruited patients baseline quality of life assessment will be done using the king’s health questionnaire which has domains like general health perceptions incontinence impact,role limitations,physical limitations,social limitations,personal relationships,emotions,sleep/energy and severity of symptoms and scoring will be given.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 90.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • women willing to participate women compliant for follow up after 3 months women presenting to the opd with complaints of urinary incontinence for the first time.

Exclusion Criteria

  • women not willing to participate women non compliant for follow up women presenting to the opd with already diagnosed or treated urinary incontinence.

Outcomes

Primary Outcomes

its a simple and doable algorithm

Time Frame: 3 months

It gives a workable and specific diagnosis before examination and investigation as it is history based

Time Frame: 3 months

change in the quality of life after 3 months on the basis of evaluation and management for tentative diagnosis as per proposed algorithm

Time Frame: 3 months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Not provided
Responsible Party
Principal Investigator
Principal Investigator

DRSamyuktha

Kasturba medical college

Study Sites (1)

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