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Not yet recruiting NCT06948604

Impact of Kegel Exercise on Patient Outcomes Post TURP

No phase Interventional BPH (Benign Prostatic Hyperplasia)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise.
Who it may be relevant to
Registry conditions: BPH (Benign Prostatic Hyperplasia). Basic parameters: 45 years — 65 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Impact of Kegel Exercises on the Postoperative Outcomes of Patients Undergoing Transurethral Resection of the Prostate

Overview

how kegel exercise will improve patient outcomes by reducing post TURP LUTs , improve patient performance status and improve patient self esteem

Detailed description

patients will divided in to two group study and control, study group will perform kegel exercise postoperative and follow patient progress at 1, 3,6 month while control group receive routine care

Interventions

  • Behavioral Exercise
    this exercise used to improve urine complication post TURP

Primary outcome measures

  • International Prostate Symptom Score [Time frame: within 3 month]
Secondary outcome measures (1)
  • World Health Organization Performance Status Scale [Time frame: within 6 month]

Eligibility criteria

Inclusion criteria

  • patient diagnosed with BPH and undergoing TURP
  • Patient age range from 45-65years old
  • Patient understand verbal and written instructions

Exclusion criteria

Patient confirmed diagnosis with prostate cancer (biopsy-PSA) Conversion to open prostatectomy Patient has cognitive impairment Patient has chronic cough /chronic bronchitis or asthma

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06948604 · kegel exercise and TURP outcom

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗