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A study to evaluate the occurrence of discomfort and pain related to the urinary catheter in patients undergoing cancer surgery

Catheter Related Bladder Discomfort (CRBD) in oncological surgeries – incidence and impact of multimodal analgesia – a single center, prospective, observational study. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/02/063050
Enrollment
250
Registered
2024-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: Nil: NA Control Intervention1: Nil: NA

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients more than or equal to 18 years of age. 2.Patients undergoing oncological surgeries under general anesthesia and needing urinary catheterization.

Exclusion criteria

Exclusion criteria: 1.Patients unwilling to participate in the study. 2.Patients catheterized prior to surgery. 3.Multiple attempts at catheterization. 4.Urogenital and pelvic surgeries. 5.Surgeries with cognitive impairment in the post-operative period (neurosurgeries) 6.Patients shifted for elective ventilation (for more than 12 hrs.) in the immediate post-operative period. 7.Since very few patients undergo surgery under spinal +/- epidural anesthesia, these patients will be excluded to avoid too many confounding factors.

Design outcomes

Primary

MeasureTime frame
Observation of incidence of CRBD in the post operative period in oncological surgeries where multimodal analgesia is used.Timepoint: In the post-operative period

Secondary

MeasureTime frame
1.To assess the severity of CRBD in the immediate post-operative period (first 24 hrs.) 2.To understand correlation between Morphine Equivalent (ME) for surgical pain and incidence of CRBD in the peri-operative period. 3.Disparity in incidence of CRBD when using the CRBD scale and NRS scale 4.To understand the treatment offered to patients complaining of CRBD and its effect on reduction of the severity of CRBD. Timepoint: In the post-operative period

Countries

India

Contacts

Public ContactDr Mugdha Satao

Tata Memorial Centre

sumitrabakshi@yahoo.in9869334449

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026